One-step method for producing adenoviral vectors

ABSTRACT

The disclosure is directed to a gene transfer vector which comprises (i) all or part of a viral genome and (ii) a suicide gene flanked by unique cloning sequences. The disclosure also is directed to a system for producing an adenoviral vector comprising a destination vector comprising (i) all or part of an adenoviral genome and (ii) a suicide gene flanked by unique cloning sequences; a transgene flanked by unique cloning sequences; and (c) reagents for Gibson DNA Assembly (GDA). A method of producing an adenoviral vector using the aforementioned system also is provided.

SEQUENCE LISTING

The text of the computer readable sequence listing filed herewith, titled “39710-202_SEQUENCE_LISTING”, created Aug. 12, 2022, having a file size of 7,473 bytes, is hereby incorporated by reference in its entirety.

BACKGROUND

Adenovirus (Ad) has received significant attention as an in vitro and in vivo gene delivery vehicle for several decades due to its well-defined virology and biology, its non-integrating property and viral genetic stability, its high gene transduction efficiency, and its ease of large-scale production (1-4). In fact, adenoviral vectors are not only used to deliver and express transgenes, but also are employed to express siRNAs for gene silencing and/or CRISPR/Cas and designer nucleases systems for genome editing (1,4,5). Adenovirus is a nonenveloped, linear double-stranded DNA virus. In humans, there are more than 50 identified serotypes, which are divided into 6 subgroups (A through G) based on their tropisms (1-4). Adenoviral capsids, which are comprised of capsid proteins, core proteins, and cement proteins, delineate tropisms among serotypes, and thus give rise to a vast range of therapeutic candidate viruses (1-4).

Compared with other viral vectors used for gene delivery, adenoviral vectors offer several distinct advantages (1-3). First, adenovirus is one of the most effective and non-integrating gene delivery systems in vitro and in vivo since most mammalian cells express the primary adenovirus receptor and secondary integrin receptors. Second, Ad vectors provide a versatile platform to modify viral capsids in order to enhance therapeutic properties and improve targeting specificity of the virus. Third, well-understood Ad virology and extensive experience with Ad vectors in preclinical and clinical applications make Ad vectors one of the most commonly used viral vectors in clinical trials worldwide. Fourth, the development of the third-generation gutless Ad vectors circumvents host anti-Ad immunity. Finally, even inherent shortcomings of adenovirus (e.g., evoked host immunity) have proven beneficial for anticancer immunotherapies, vaccination, and/or oncolytic therapies.

Despite the widespread use of adenoviral vectors, the construction and propagation of adenoviral vectors remains a technically challenging and time-consuming process. Thus, there is a need for improved systems and methods for producing adenoviral vectors.

BRIEF SUMMARY OF THE DISCLOSURE

The disclosure provides a gene transfer vector comprising (i) all or part of a viral genome and (ii) a suicide gene flanked by a first cloning nucleic acid sequence and a second cloning nucleic acid sequence, wherein the first and second cloning nucleic acid sequences are different.

The disclosure also provides system for producing an adenoviral vector, which comprises: (a) a destination vector comprising (i) all or part of an adenoviral genome and (ii) a suicide gene flanked by a first cloning nucleic acid sequence and a second cloning nucleic acid sequence, wherein the first and second cloning nucleic acid sequences are different; (b) a transgene flanked the first cloning nucleic acid sequence and the second cloning nucleic acid sequence; and (c) reagents for Gibson DNA Assembly (GDA). A method of producing an adenoviral vector using the aforementioned system also is provided.

BRIEF DESCRIPTION OF THE DRAWING(S)

FIGS. 1A and B show a schematic depiction of the one-step construction of adenovirus (OSCA) system using the Gibson DNA Assembly technology. (A) Construction of the destination/recipient vectors for the OSCA system. Two unique sequences MOS1 and MOS2, flanking the unique SwaI site, were first engineered in a first-generation adenoviral shuttle vector, resulting in pShuttle-MOS (i). Linearized pShuttle-MOS was transformed into the pAdEasy-1-containing BJ5183 bacterial cells and selected for Kan-resistant pAdOS plasmid (ii), which was subsequently confirmed by PCR and sequencing. The ccdB gene fragment flanked with SwaI sites was assembled to the SwaI-linearized pAdOS through Gibson Assembly and grown in DB3.1 bacterial cells, resulting in the OSCA destination/recipient pAdOSd vector (iii). Two alternative destination vectors pAdGOSd and pAdROSd, which co-express GFP and RFP, respectively, were constructed in a similar fashion (FIGS. S1 and S2). (B) Gibson Assembly-mediated one-step construction of recombinant adenoviruses. The coding region of the gene of interest (GOI) is first PCR amplified with MOS1 and MOS2-anchored primers (i), and the purified PCR fragment is assembled with the SwaI-digested destination vector, e.g., pAdOSd, pAdGOSd, or pAdROSd, through Gibson Assembly reactions (ii). The resultant plasmids are verified, linearized by PacI digestion, and transfected into packaging cells such as 293pTP, leading to robust adenovirus generation in 5-7 days (iii). The adenoviral lysate can be further amplified in HEK-293 cells to accomplish high titers.

FIGS. 2A-D illustrate the construction and characterization of copGFP expressing adenoviral vector using the OSCA system. (A) Construction of AdOS-copGFP using the OSCA system. The copGFP coding sequence was PCR amplified with MOS1 and MOS2 anchored primers (i), followed by Gibson Assembly (ii). (B) Bacterial colonies post the Gibson Assembly reaction. (C) Identification of pAdOS-copGFP using PCR screening of bacterial colonies. Randomly picked up 16 colonies were PCR amplified with copGFP specific primers, and all but one (#11) were positive for copGFP. (D) Validation of adenoviral recombinant pAdOScopGFP clones. The representative three clones, along with the control adenoviral backbone vector pAdEasy1, were digested with Hind III (i), Kpn I (ii), Bam HI (iii), and Sph I (iv). The digested plasmid DNA was resolved in 1% agarose gels.

FIGS. 3A and B illustrate packaging and production of recombinant adenoviruses generated from the Gibson Assembly technology. (A) The initial production of AdOS-copGFP virus in 293pTP cells. At the indicated time points, GFP signal was also recorded. Comet-like adenovirus-producing foci were apparent at 5 days after transfection. Representative images are shown. Both GFP and bright field images were also recorded at a lower magnification (4×) (FIG. S3A). (B) Transduction efficiency of adenoviral lysate. The collected adenoviral lysate was used to infect subconfluent HEK-293 cells at the indicated viral titers (% of viral lysate volume).

FIGS. 4A-D illustrate the construction and production of mouse BMP9-expressing adenovirus vector using the OSCA system. (A) Packaging and production of recombinant adenoviruses generated from the Gibson Assembly technology. The coding region of mouse BMP9 was PCR amplified with gene-specific primers containing MOS1 and MOS2 sequences (i), and Gibson assembled with SwaI-digested pAdROSd vector to generate pAdROS-mBMP9 (ii). (B) Bacterial colony verification. The Gibson Assembly product was transformed into DH10B (i) and subjected to colony PCR with BMP9-specific primers (ii). (C) Packaging of AdROS-mBMP9 in 293pTP cells. At the indicated time points, RFP signal was also recorded. Comet-like adenovirus-producing foci were apparent at 5 days after transfection. Representative images are shown. Both RFP and bright field images were also recorded at a lower magnification (4×) (FIG. 8B). (D) Transduction efficiency of AdROS-mBMP9 in mesenchymal stem cells. Subconfluent imBMSC cells were infected with the indicated titers of AdROS-mBMP9, and RFP signal was recorded at 36 h post infection. Representative images are shown. MOI, multiplicity of infection, indicating # of infectious adenoviruses per cell.

FIGS. 5A-C demonstrate that adenovirus-mediated BMP9 transgene expression induces osteogenic differentiation of mesenchymal stem cells (MSCs). (A) Adenovirus-mediated expression of BMP9 effectively induces osteogenic marker alkaline phosphatase (ALP) in MSCs. Mouse imBMSCs were infected with AdROS-mBMP9 or Ad-RFP. At the indicated time points, the ALP activities of the infected cells were assessed histochemically (i) and quantitatively (ii). “*” p<0.01, compared with respective RFP group. (B) Adenovirus-mediated expression of BMP9 effectively induces matrix mineralization in MSCs. AdROSmBMP9 or Ad-RFP infected imBMSCs were cultured in mineralization medium and subjected to Alizarin Red S staining at the indicated time points. Representative results are shown. (C) Adenovirus-mediated expression of BMP9 effectively induces ectopic bone formation in MSCs. Subconfluent imBMSCs were infected with AdROS-mBMP9 or Ad-RFP (i). The infected cells were collected and injected subcutaneously into athymic nude mice. While no masses were formed in the Ad-RFP group, bony masses were retrieved from the AdROS-mBMP9 group at 4 weeks after implantation and subjected to H&E staining (ii) and Masson's trichrome staining (iii). Representative results are shown.

FIG. 6 is a vector map of the pAdGOSd vector, a destination vector for Gibson assembly-mediated one-step construction of recombinant adenovirus. The pAdGOSd vector co-expresses eGFP marker.

FIG. 7 is a vector map of the pAdROSd vector, a destination vector for Gibson assembly-mediated one-step construction of recombinant adenovirus. The pAdROSd vector co-expresses mRFP marker.

FIG. 8A-B shows packaging and production of recombinant adenoviruses generated from the Gibson Assembly technology. (A) The initial production of AdOS-copGFP virus in 293pTP cells. At the indicated time points, both GFP and bright field (BF) images were recorded at lower magnification (4×). Comet-like images were apparent at 5 days after transfection. Representative images are shown. (B) The initial production of AdROS-mBMP9 virus in 293pTP cells. At the indicated time points, both RFP and bright field (BF) images were recorded at lower magnification (4×). Comet-like images were apparent at 5 days after transfection. Representative images are shown.

DETAILED DESCRIPTION

The present disclosure is predicated, at least in part, on the development of a simplified system and method for constructing adenoviral vectors using Gibson DNA Assembly (GDA). In some embodiments, the disclosure provides adenoviral recipient vectors that contain two unique 20-base pair (bp) cloning nucleic acid sequences that serve as universal overlapping sites for Gibson Assembly reactions at a deleted E1 region of the adenovirus genome. In other embodiments, the recipient adenoviral vectors further comprise a bacterial suicide gene located between the cloning nucleic acid sequences to reduce cloning background.

Gene Transfer Vector

The disclosure provides a gene transfer vector comprising (i) all or part of a viral genome and (ii) a suicide gene flanked by a first cloning nucleic acid sequence and a second cloning nucleic acid sequence, wherein the first and second cloning nucleic acid sequences are different. The term “gene transfer vector,” as used herein, refers to a vehicle used to deliver foreign genetic material to a cell, where it can be replicated and/or expressed. Gene transfer vectors ideally enter a wide variety of cell types, have the capacity to accept large nucleic acid sequences, are safe, and can be produced in quantities required for treating patients. Any gene transfer vector can be employed in the present disclosure, including viral and non-viral gene transfer vectors. Examples of suitable viral gene transfer vectors include, but are not limited to, retroviral vectors, adeno-associated virus vectors, vaccinia virus vectors, herpesvirus vectors, parainfluenza-RSV chimeric vectors (PIV-RSV), and adenoviral vectors. Examples of suitable non-viral vectors include, but are not limited to, plasmids, liposomes, and molecular conjugates (e.g., transferrin).

In some embodiments, the gene transfer vector is a viral vector, which comprises all or part of a viral genome. For example, the gene transfer vector may comprise all or part of an adenovirus genome, which is referred to as an “adenoviral vector.” Adenovirus is a medium-sized (90-100 nm), nonenveloped icosahedral virus containing approximately 36 kilobases (kb) of double-stranded DNA. The term “adenovirus,” as used herein, refers to an adenovirus that retains the ability to participate in the adenovirus life cycle and has not been physically inactivated by, for example, disruption (e.g., sonication), denaturing (e.g., using heat or solvents), or cross-linkage (e.g., via formalin cross-linking). The “adenovirus life cycle” includes (1) virus binding and entry into cells, (2) transcription of the adenoviral genome and translation of adenovirus proteins, (3) replication of the adenoviral genome, and (4) viral particle assembly (see, e.g., Fields Virology, 5th ed., Knipe et al. (eds.), Lippincott Williams & Wilkins, Philadelphia, Pa. (2006)). The term “adenoviral vector,” as used herein, refers to an adenovirus in which the adenoviral genome has been manipulated to accommodate a nucleic acid sequence that is non-native with respect to the adenoviral genome. Typically, an adenoviral vector is generated by introducing one or more mutations (e.g., a deletion, insertion, or substitution) into the adenoviral genome of the adenovirus so as to accommodate the insertion of a non-native nucleic acid sequence, for example, for gene transfer, into the adenovirus.

Several features of adenoviruses make them ideal vehicles for transferring genetic material to cells for therapeutic applications (e.g., gene therapy, immunotherapy, or as vaccines). For example, adenoviruses can be produced in high titers (e.g., about 10¹³ particle units (pu)), and can transfer genetic material to nonreplicating and replicating cells. The adenoviral genome can be manipulated to carry a large amount of exogenous DNA (up to about 8 kb), and the adenoviral capsid can potentiate the transfer of even longer sequences (Curiel et al., Hum. Gene Ther., 3: 147-154 (1992)). Additionally, adenoviruses generally do not integrate into the host cell chromosome, but rather are maintained as a linear episome, thereby minimizing the likelihood that a recombinant adenovirus will interfere with normal cell function.

The adenovirus capsid mediates the key interactions of the early stages of the infection of a cell by the virus and is required for packaging adenovirus genomes at the end of the adenovirus life cycle. The capsid comprises 252 capsomeres, which includes 240 hexon trimers, 12 penton base pentamer proteins, and 12 trimer fibers (Ginsberg et al., Virology, 28: 782-83 (1966)). The hexon comprises three identical proteins, namely polypeptide II (Roberts et al., Science, 232: 1148-51 (1986)). The penton base comprises five identical proteins and the fiber comprises three identical proteins. Proteins Ma, VI, and IX are present in the adenoviral coat and are believed to stabilize the viral capsid (Stewart et al., Cell, 67: 145-54 (1991), and Stewart et al., EMBO J., 12(7): 2589-99 (1993)). The expression of the capsid proteins, with the exception of pIX, is dependent on the adenovirus polymerase protein. Therefore, major components of an adenovirus particle are expressed from the genome only when the polymerase protein gene is present and expressed.

The adenoviral vector may be of any serotype or combination of serotypes. Over 50 serotypes of adenovirus have been identified, which are classified as subgroup A (e.g., serotypes 12, 18, and 31), subgroup B (e.g., serotypes 3, 7, 11, 14, 16, 21, 34, 35, 50, and 55), subgroup C (e.g., serotypes 1, 2, 5, and 6), subgroup D (e.g., serotypes 8, 9, 10, 13, 15, 17, 19, 20, 22-30, 32, 33, 36-39, and 42-49, 51, 53, 54, 56), subgroup E (e.g., serotype 4), subgroup F (e.g., serotypes 40 and 41), subgroup G (e.g., serotype 52). Various serotypes of adenovirus are available from the American Type Culture Collection (ATCC, Manassas, Va.). In one embodiment, the adenovirus or adenoviral vector is a serotype 5 adenovirus or adenoviral vector (“Ads”).

The adenoviral vector can be replication-deficient or conditionally replication-competent. An adenoviral vector that is “replication-competent” can replicate in typical host cells, i.e., cells typically capable of being infected by an adenovirus. In contrast, a “replication-deficient” or “replication-incompetent” adenoviral vector requires complementation of one or more gene functions or regions of the adenoviral genome that are required for replication, as a result of, for example, a deficiency in one or more replication-essential gene function or regions, such that the adenovirus or adenoviral vector does not replicate in typical host cells, especially those in a human to be infected by the adenovirus or adenoviral vector.

A “conditionally-replicating” adenovirus or adenoviral vector is an adenovirus or adenoviral vector that has been engineered to replicate under pre-determined conditions. For example, replication-essential gene functions, e.g., gene functions encoded by the adenoviral early regions, can be operably linked to an inducible, repressible, or tissue-specific promoter. In such embodiments, replication requires the presence or absence of specific factors that activate or repress the promoter. Conditionally-replicating adenoviral vectors are further described in, e.g., U.S. Pat. Nos. 5,998,205 and 6,824,771.

A deficiency in a gene function or genomic region, as used herein, is defined as a disruption (e.g., deletion) of sufficient genetic material of the adenoviral genome to obliterate or impair the function of the gene (e.g., such that the function of the gene product is reduced by at least about 2-fold, 5-fold, 10-fold, 20-fold, 30-fold, or 50-fold) whose nucleic acid sequence was disrupted (e.g., deleted) in whole or in part. Deletion of an entire gene region often is not required for disruption of a replication-essential gene function. However, for the purpose of providing sufficient space in the adenoviral genome for one or more transgenes, removal of a majority of one or more gene regions may be desirable. While deletion of genetic material is preferred, mutation of genetic material by addition or substitution also is appropriate for disrupting gene function. Replication-essential gene functions are those gene functions that are required for adenovirus replication (e.g., propagation) and are encoded by, for example, the adenoviral early regions (e.g., the E1, E2, and E4 regions), late regions (e.g., the L1, L2, L3, L4, and L5 regions), genes involved in viral packaging (e.g., the IVa2 gene), and virus-associated RNAs (e.g., VA-RNA-1 and/or VA-RNA-2).

The early region 1A and 1B (E1A and E1B) genes encode proteins required for a productive adenovirus lytic cycle (Fields, supra). E1A is the first viral gene transcribed after infection and produces two related proteins, 243R and 289R, which induce transcription of the other early viral gene regions and stimulate infected cells to enter S-phase of the cell cycle. The E1B region encodes two major proteins, E1B19K and E1B55K. The E1B55K protein binds the cellular tumor suppressor p53 and can block p53-mediated apoptosis and inhibition of viral and cellular replication. The E1B19K protein is a Bcl-2 homologue that interacts with Bax and inhibits apoptosis, allowing the virus to replicate longer (Sundararajan, R. and White, E, J. Virology, 75:7506-7516 (2001)). The E1A proteins have been shown to induce S-phase in infected cells by associating with p300/CBP or the retinoblastoma (Rb) protein (Howe et al., Proc. Natl. Acad. Sci. USA, 87: 5883-5887 (1990); Wang et al., Mol. Cell. Biol., 11: 4253-4265 (1991); Howe, J. A. and Bayley, S. T. Virology, 186: 15-24 (1992)). Rb and p300 regulate the activity of E2F transcription factors, which coordinate the expression of cellular genes required for cell cycle progression (Helin, K., Curr. Opin. Genet. Dev., 8: 28-35 (1998)). Thus, E1A gene products play a role in viral genome replication by driving entry of quiescent cells into the cell cycle, in part, by displacing E2F transcription factors from the retinoblastoma protein (pRb) tumor suppressor (Liu, X. and Marmorstein, R., Genes & Dev., 21: 2711-2716 (2007)).

In some embodiments, the adenoviral vector may comprise a deletion, in whole or in part, of one or more regions of the adenoviral genome. In some embodiments, the adenoviral vector comprises a deletion of sufficient genetic material of the adenoviral genome to obliterate or impair the function of the gene (e.g., such that the function of the gene product is reduced by at least about 2-fold, 5-fold, 10-fold, 20-fold, 30-fold, or 50-fold) whose nucleic acid sequence was disrupted (e.g., deleted) in whole or in part. For the purpose of providing sufficient space in the adenoviral genome for one or more non-native nucleic acid sequences (or “transgenes”), removal of a majority of one or more gene regions may be desirable. In this regard, the adenovirus or adenoviral vector may comprise a deletion of all or part of any of the adenoviral early regions (e.g., E1, E2, E3 and E4 regions), the late regions (e.g., the L1, L2, L3, L4, and L5 regions), genes involved in viral packaging (e.g., the IVa2 gene), and/or virus-associated RNAs (e.g., VA-RNA-1 and/or VA-RNA-2). In one embodiment, the adenoviral vector comprises a deletion of all or part of the E1A region, a deletion of all or part of the E1B region of the adenoviral genome, a deletion of all or part of the E3 region of the adenoviral genome, and/or a deletion of all or part of the E4 region of the adenoviral genome. The size of the deletion may be tailored so as to retain an adenoviral vector whose genome closely matches the optimum genome packaging size. A larger deletion will accommodate the insertion of larger non-native nucleic acid sequences in the adenoviral genome.

First-generation adenoviral vectors (“Ad vectors”) are deficient in the E1 region (i.e., E1A and E1B) and E3 region, with an initial transgene cloning capacity of 5.2 kb (1). Second-generation Ad vectors are deficient in more non-structural genes (e.g., E2/E4) in addition to the E1 and E3 regions, leading to increased cloning capacity and decreased cytotoxicity, although these Ad vectors require distinct packaging cells for viral production (1). Third-generation Ad vectors (also known as high-capacity adenoviral vectors (HC-AdVs), gutless AdVs, or helper-dependent AdVs (HD-AdVs)) are deficient in all viral coding sequences, containing only 5′ and 3′ ITRs and the packaging signal, thus providing a larger capacity for transgenic cloning sequences (36 kb) (1). While HCAdVs offer many benefits with significantly minimized cytotoxicity, their production depends on the presence of a helper adenovirus genome provided in trans, which often compromises virus quantities.

By removing all or part of certain regions of the adenoviral genome, for example, the E1B, E3, and/or E4 regions of the adenoviral genome, the resulting adenoviral vector is able to accept inserts of exogenous non-native nucleic acid sequences while retaining the ability to be packaged into adenoviral capsids. Thus, in another embodiment, the adenoviral vector comprises one or more non-native nucleic acid sequences. A non-native nucleic acid sequence can be inserted at any position in the adenoviral genome so long as insertion allows for the formation of adenovirus or the adenoviral vector particle. A “non-native” nucleic acid sequence is any nucleic acid sequence (e.g., DNA, RNA, or cDNA sequence) that is not a naturally occurring nucleic acid sequence of an adenovirus in a naturally occurring position. The terms “non-native nucleic acid sequence,” “heterologous nucleic acid sequence,” and “exogenous nucleic acid sequence” are synonymous and can be used interchangeably in the context of the present disclosure. The non-native nucleic acid sequence preferably is DNA and preferably encodes a protein (e.g., one or more nucleic acid sequences encoding one or more proteins). The term “transgene” is defined herein as a non-native nucleic acid sequence that is operably linked to appropriate regulatory elements (e.g., a promoter), such that the non-native nucleic acid sequence can be expressed to produce an RNA or protein (e.g., a regulatory RNA sequence, peptide, or polypeptide). The regulatory elements (e.g., promoter) can be native or non-native to the adenovirus or adenoviral vector.

To facilitate selection of vectors containing a transgene or gene of interest (GOI), the gene transfer vector further comprises a suicide gene. The term “suicide gene,” as used herein, refers to a gene whose expression is lethal to a cell in which it is expressed. While an understanding of a mechanism is not needed to practice the present disclosure and while the disclosure is not limited to any particular mechanism, the presence of a suicide gene in the gene transfer vector allows for the selection of cells in which the suicide gene is replaced by a transgene of interest during vector construction, which is an indication of successful vector production. In other words, the presence of the suicide gene allows for selection against vectors that do not incorporate the transgene of interest. Any suitable suicide gene may be incorporated into the gene transfer vector. Suitable suicide genes include, but are not limited to, the cytosine deaminase gene (CD) of Escherichia coli, the herpes simplex virus thymidine kinase gene (HSV-tk), and the bacterial suicide gene ccdB. In some embodiments, the suicide gene is a ccdB gene.

In nature, the ccdB gene is located on the F sex factor plasmid of E. coli and is part of a toxin-antitoxin system encoded by the ccd operon, which is responsible for plasmid maintenance during cell division. ccdB codes for a toxic protein (CcdB) that acts as a DNA gyrase poison, locking up DNA gyrase with broken double stranded DNA and ultimately causing cell death. The ccdB gene has been used as a positive selection gene in recombinant DNA and molecular cloning methodologies for over 25 years (see, e.g., Bernard, P., Biotechniques, 21(2): 320-3 (1996); Bahassi et al., Mol Microbiol., 15(6): 1031-7 (1995); and Bernard et al., Gene, 148(1):71-4 (1994)).

In some embodiments, the suicide gene is flanked by a first cloning nucleic acid sequence and a second cloning nucleic acid sequence to facilitate vector construction and transgene cloning. The first cloning nucleic acid sequence and second cloning nucleic acid sequence desirably are different. Each of the first and second cloning nucleic acid sequences may be of any suitable size. For example, each of the first and second cloning nucleic acid sequences may be greater than five nucleotides (e.g., 6, 7, 8, 9, or 10 nucleotides), but desirably less than 30 nucleotides (e.g., 29, 25, or 20 nucleotides). In some embodiments, each of the first and second cloning nucleic acid sequences comprises about 15-25 nucleotides (e.g., 16, 17, 18, 19, 20, 21, 22, 23, or 24 nucleotides). In other embodiments, each of the first and second cloning nucleic acid sequences comprises about 20 nucleotides. An exemplary first cloning nucleic acid sequence comprises SEQ ID NO: 1 (AATCGGAAAGCGGACGCGGA), and an exemplary second cloning nucleic acid sequence comprises SEQ ID NO: 2 (CGAGTATCCCGTGAGCGCTT). The disclosure is not limited to these particular cloning nucleic acid sequences, however.

Compositions

The disclosure further provides a composition comprising the gene transfer vector (e.g., an adenoviral vector) described herein and a carrier therefor (e.g., a pharmaceutically acceptable carrier). The composition desirably is a physiologically acceptable (e.g., pharmaceutically acceptable) composition, which comprises a carrier, preferably a physiologically (e.g., pharmaceutically) acceptable carrier, and the gene transfer vector. Any suitable carrier can be used within the context of the disclosure, and such carriers are well known in the art. The choice of carrier will be determined, in part, by the particular use of the composition (e.g., administration to an animal) and the particular method used to administer the composition. In some embodiments, the pharmaceutical composition can be sterile.

Suitable compositions include aqueous and non-aqueous isotonic sterile solutions, which can contain anti-oxidants, buffers, and bacteriostats, and aqueous and non-aqueous sterile suspensions that can include suspending agents, solubilizers, thickening agents, stabilizers, and preservatives. The composition can be presented in unit-dose or multi-dose sealed containers, such as ampules and vials, and can be stored in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example, water, immediately prior to use. Extemporaneous solutions and suspensions can be prepared from sterile powders, granules, and tablets. Preferably, the carrier is a buffered saline solution. More preferably, the gene transfer vector is part of a composition formulated to protect the gene transfer vector from damage prior to administration. For example, the composition can be formulated to reduce loss of the gene transfer vector on devices used to prepare, store, or administer the adenoviral vector, such as glassware, syringes, or needles. The composition can be formulated to decrease the light sensitivity and/or temperature sensitivity of the gene transfer vector. For example, when the gene transfer vector is an adenoviral vector, the composition may comprise a pharmaceutically acceptable liquid carrier, such as, for example, those described above, and a stabilizing agent selected from the group consisting of polysorbate 80, L-arginine, polyvinylpyrrolidone, trehalose, and combinations thereof. Use of such a composition will extend the shelf life of the adenovirus or adenoviral vector and facilitate its administration. Formulations for adenoviral vector-containing compositions are further described in, for example, U.S. Pat. Nos. 6,225,289, 6,514,943, 7,456,009, 7,888,096; 10,272,032 and International Patent Application Publication WO 2000/034444.

Systems and Methods for Producing Adenoviral Vectors

The disclosure further provides systems and methods for producing an adenoviral vector. In some embodiments, the system comprises (a) a destination vector comprising (i) all or part of an adenoviral genome and (ii) a suicide gene flanked by a first cloning nucleic acid sequence and a second cloning nucleic acid sequence, wherein the first and second cloning nucleic acid sequences are different; (b) a transgene comprising a nucleic acid sequence flanked the first cloning nucleic acid sequence and the second cloning nucleic acid sequence; and (c) reagents for Gibson DNA Assembly (GDA). The destination vector may comprise all or a part of an adenoviral genome, as described herein. For example, the destination vector may be an adenoviral vector of any serotype (such as serotype 5) comprising a deletion of the E1 region, and optionally deletions in other early and/or late region genes. Descriptions of the suicide gene, first and second cloning nucleic acid sequences, transgene, and components thereof set forth above in connection with the gene transfer vector also are applicable to those same aspects of the aforementioned system and method.

Gibson DNA Assembly (GDA), named after its developer Daniel G. Gibson (14), is a synthetic biology technique that allows the one-step isothermal DNA assembly of multiple overlapping fragments in a restriction enzyme-free, seamless, and sequence-independent fashion. A typical GDA in vitro recombination system contains three essential isothermal enzymes: 5′-exonuclease to remove nucleotides from the ends of double-stranded DNA molecules and expose complementary single-stranded DNA (ssDNA) overhangs for specific annealing; DNA polymerase to fill in the ssDNA gaps of the joined molecules; and DNA ligase to covalently seal the nicks (15). The GDA method is a useful molecular engineering tool to construct synthetic and natural genes, genetic pathways, and entire genomes (14-16). The GDA method also has been used to generate adenoviral vectors (see, e.g., Pan et al., Viruses 2018 Oct. 18; 10(10):568. doi: 10.3390/v10100568; Zou et al., J Virol Methods 2018 July; 257:85-92. doi: 10.1016/j.jviromet.2018.04.001; Miciak et al., PLoS ONE 13(6): e0199563 (2018). doi.org/10.1371/journal.pone.0199563; and Hamdan et al., Molecular Therapy: Methods & Clinical Development, 20: P625-634 (2021)). Reagents for Gibson DNA Assembly include, but are not limited to 5′-exonucleases (e.g., T5 exonuclease), DNA polymerases (e.g., Phusion DNA polymerase), DNA ligases (e.g., Taq DNA ligase), host cells (e.g., competent E. coli cells), and cell culture media.

The disclosure also provides a method of producing an adenoviral vector comprising contacting a cell with the above-described system. Recombinant adenoviral vectors typically are generated using one of four different approaches. The first method developed involves homologous recombination between a shuttle vector and an backbone adenovirus genome vector in packaging cells such as HEK-293 cells (1,6), but suffers from extremely low efficiency. An alternative technique is the direct ligation of transgene-containing fragments to a linearized E1/E3-deleted adenoviral genome DNA fragment using several restriction enzymes, such as ClaI, I-CeuI, SwaI and PI-SceI engineered in the E1 deletion region (7). This ligation approach, however, is rarely used due to low efficiency and the recombinant virus often requires purification from contaminating wild-type transgene-null Ad viruses. A third approach involves the use of site-specific recombinase and transposase systems, such as the CRE/LOX and FLIP/FRT recombinases and the GATEWAY® transposon system, to insert transgenes into the E1 deletion region at specific recipient sites (8,9). However, these systems are extensively commercialized with high cost and lack of technical transparency, which limits their widespread use. The fourth approach involves taking advantage of more efficient homologous recombination in microorganisms, such as bacteria and yeast, to generate transgene-containing adenoviral vectors (10-13). An example of such a system is the AdEasy system, which has become one of the most commonly used techniques worldwide to generate Ad vectors (1,2,12,13). An essential component of the AdEasy system is the RecA⁺ E. coli strain BJ5183, which exhibits a high rate of homologous recombination but allows for the generation of stable large recombinants (1,12,13). BJ5183 cells, however, exhibit a relatively low transformation efficiency compared with conventional strains used for molecular cloning, which poses technical challenges to researchers. Certain components of the AdEasy system may be used in the connection with the disclosed system and method. Methods for the production and purification of adenoviruses and adenoviral vectors are described in, e.g., U.S. Pat. No. 6,194,191, and International Patent Application Publications WO 99/54441, WO 98/22588, WO 98/00524, WO 96/27677, and WO 2003/078592.

Production of adenoviral vectors also may involve the use of complementing cell lines. The term “complementing cell lines,” as used herein, refers to cell lines that provide gene functions not present in a replication-deficient adenoviral vector, but required for viral propagation, at appropriate levels in order to generate high titers of viral vector stock. Such complementing cell lines are known and include, but are not limited to, 293 cells (described in, e.g., Graham et al., J. Gen. Virol., 36: 59-72 (1977)) and PER.C6 cells (described in, e.g., International Patent Application Publication WO 1997/000326, and U.S. Pat. Nos. 5,994,128 and 6,033,908). It has been shown that overexpression of serotype 5 adenovirus precursor terminal protein (pTP) alone, or in combination with E1A overexpression, in HEK-293-based cells, namely 293pTP and RAPA cell lines, respectively, accelerates Ad packaging and amplification processes (17,18). Thus, in some embodiments, the above described system may be introduced into cells that overexpress pTP and/or E1A. In some instances, one or more replication-essential gene functions lacking in a replication-deficient adenoviral vector can be supplied by a helper virus, e.g., an adenoviral vector that supplies in trans one or more essential gene functions required for replication of the replication-deficient adenoviral vector.

The use of the terms “a” and “an” and “the” and “at least one” and similar referents in the context of describing the invention (especially in the context of the following claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. The use of the term “at least one” followed by a list of one or more items (for example, “at least one of A and B”) is to be construed to mean one item selected from the listed items (A or B) or any combination of two or more of the listed items (A and B), unless otherwise indicated herein or clearly contradicted by context. The terms “comprising,” “having,” “including,” and “containing” are to be construed as open-ended terms (i.e., meaning “including, but not limited to,”) unless otherwise noted. Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., “such as”) provided herein, is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the invention.

Preferred embodiments of this invention are described herein, including the best mode known to the inventors for carrying out the invention. Variations of those preferred embodiments may become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventors expect skilled artisans to employ such variations as appropriate, and the inventors intend for the invention to be practiced otherwise than as specifically described herein. Accordingly, this invention includes all modifications and equivalents of the subject matter recited in the claims appended hereto as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or otherwise clearly contradicted by context.

The following examples further illustrate the invention but, of course, should not be construed as in any way limiting its scope.

EXAMPLES

The following materials and methods were used in the experiments described in the Examples.

Cell Culture, Enzymes and Chemicals

Human HEK-293 derivative lines 293pTP and RAPA cells were used for adenovirus packaging and amplification as previously described (17,18). Mouse bone marrow-derived mesenchymal stem cells imBMSCs were previously characterized (19). All cells were maintained in DMEM supplemented with 10% fetal bovine serum (FBS, Gemini Bio-Products), 100 U/ml penicillin, and 100 μg/ml streptomycin at 37° C. in 5% CO₂ as described previously (20-22). All restriction endonucleases, and the Gibson Assembly Master Mix or the NEBUILDER® HiFi DNA Assembly kit were purchased from New England Biolabs (NEB, Ipswich, Mass.). Unless indicated otherwise, other chemicals were purchased from ThermoFisher Scientific (Waltham, Mass.) or Millipore Sigma (St. Louis, Mo.).

Construction of the Adenoviral Backbone-Containing GDA Recipient Vectors pAdOSd, pAdROSd, and pAdGOSd

The CMV-PA expression cassette of the pShuttle-CMV, pAdTrack-CMV, or pAdTrace-CMV shuttle vectors used in the AdEasy system (1,12,13,23) were first modified by inserting a SwaI restriction site flanked with two unique 20-bp sequences MOS1 and MOS2, resulting in the pShuttle-MOS vector (from pShuttle-CMV). This vector was linearized with PmeI and subjected to homologous recombination reactions in pAdEasyl-containing BJ5183 bacterial cells. The kanamycin-resistant colonies were grown up and verified by PCR and restriction digestion to generate the pAdOS vector.

In order to reduce the background of GDA reactions, the bacterial suicide gene ccdB expression cassette was PCR amplified with both primers anchored with SwaI sites, ligated into the SwaI-digested pAdOS vector, and transformed into competent DB3.1 bacterial cells. Bacterial colonies were PCR screened, and positive candidate clones were grown up and further verified by PCR, restriction digestions, and DNA sequencing. The resultant GDA recipient vector was designated pAdOSd. Similar recipient vectors were also constructed from pAdTrack-CMV and pAdTrace-CMV shuttle vectors, and designated pAdGOSd and pAdROSd, respectively. All oligo sequences are listed in Table 1. The vector maps and sequences for pAdGOSd and pAdROSd are shown in FIG. 6 and FIG. 7 . All cloning and assembly junctions were verified by DNA sequencing.

TABLE 1 Gene/ Oligo Name Sequence Use MOS1/2 GatccAATCGGAAAGCGGACGCGGAatt cloning cassette taaatCGAGTATCCCGTGAGCGCTTt (SEQ ID NO: 3) CtagaAAGCGCTCACGGGATACTCGatt taaatTCCGCGTCCGCTTTCCGATTg (SEQ ID NO: 4) copGFP AATCGGAAAGCGGACGCGGAatttacca GDA Forward ccATGGAGAGCGACGACAGCGGCCATG (SEQ ID NO: 5) copGFP AAGCGCTCACGGGATACTCGatttAG Reverse CGAGATCCGGTGGAGCCGGG (SEQ ID NO: 6) mouse AATCGGAAAGCGGACGCGGAatttacca BMP9 ccatgggcATGCATATGTCCCCTGGGGC Forward CTTC (SEQ ID NO: 7) mouse AAGCGCTCACGGGATACTCGatttct BMP9 acctacacccacactcagccacac Reverse (SEQ ID NO: 8) MOSO1F AATCGGAAAGCGGACGCGGAattt colony (SEQ ID NO: 9) MOSO2R AAGCGCTCACGGGATACTCGattt PCR (SEQ ID NO: 10)

Gibson DNA Assembly (GDA) Reactions

The GDA reactions were carried out by using the Gibson Assembly Master Mix or NEBUILDER® HiFi DNA Assembly kit from NEB as described (24). The coding region for the gene of interest (GOI, see below) was PCR amplified using the PHUSION® High-Fidelity PCR kit. Each assembly reaction (usually in 10-15 μl reaction volume) contained approximately 100 ng of insert DNA and 50 ng of the SwaI-linearized pAdOSd, pAdGOSd, or pAdROSd vector, and incubated at 50° C. for 40-60 minutes. After the assembly reaction was completed, the reaction mix was briefly digested with SwaI and transformed into electro-competent DH10B cells. Colony PCR screening was carried out using primers specific for the GOI. Positive clones were further sequencing verified.

Generation and Amplification of Recombinant Adenoviruses Expressing copGFP, and Mouse BMP9 (mBMP9) Using OSCA

The coding sequences for copGFP and mouse BMP9 were PCR amplified with forward primers anchored with the MOS1 and kozak sequences and reverse primers anchored with the MOS2 sequence (Table 1). The PCR fragments were gel purified and used for GDA reactions. Positive candidate clones were screened by colony PCR and validated by restriction digestions and DNA sequencing. The resultant recombinant adenovirus plasmids were designated pAdOS-copGFP and pAdROS-mBMP9, respectively.

For making recombinant adenoviruses, these plasmids were first linearized with Pad to liberate adenoviral inverted terminal repeat (ITR) sequences at both ends, and then transfected into 293pTP or RAPA cells as described (17,18). Apparent adenovirus packaging and production were obtained at 5-7 days after transfection. Adenoviral lysates were prepared by multiple cycles of freeze-thaw as described (13,23). High titer adenoviruses were obtained through repeated infections of HEK-293, 293pTP, or RAPA cells, and the resultant adenoviruses were designated as AdOS-copGFP and AdROSmBMP9, respectively. Analogous adenovirus expressing only RFP (Ad-RFP) was used as a control (25-29). For the adenoviral infections, polybrene (4-8 μg/ml) was added to enhance infection efficiency as previously reported (30).

Qualitative and Quantitative Assays of Alkaline Phosphatase (ALP) Activity

ALP activity was assessed quantitatively with a modified assay using the GREAT ESCAPE™ SEAP Chemiluminescence assay kit (BD Clontech, Mountain View, Calif.) and qualitatively with a histochemical staining assay (using a mixture of 0.1 mg/ml napthol AS-MX phosphate and 0.6 mg/ml Fast Blue BB salt), as previously described (31-34). Each assay condition was performed in triplicate and the results were repeated in at least three independent experiments.

Ectopic Bone Formation

All animal studies were conducted by following the guidelines approved by the Institutional Animal Care and Use Committee (IACUC) of The University of Chicago. Stem cell-mediated ectopic bone formation was performed as described (28,35,36). Briefly, subconfluent imBMSC cells were infected with AdROS-mBMP9 or Ad-RFP for 16 hours, collected, and resuspended in PBS for subcutaneous injection (5×10⁶/injection) into the flanks of athymic nude mice (5/group, 4-6 wk old, female, ENVIGO, Indianapolis, Ind.). At four weeks after implantation, animals were sacrificed, and the implantation sites were retrieved for histologic evaluation and Trichrome staining as described below.

Histological Analysis and Trichrome Staining

Retrieved tissues were fixed, decalcified in 10% buffered formalin, and embedded in paraffin. Serial sections of the embedded specimens were stained with hematoxylin and eosin (H & E). Trichrome staining was carried out as previously described (37-41).

Statistical Analysis

Quantitative ALP assays were performed in triplicate. Data were expressed as mean±SD. Statistical significances were determined by one-way analysis of variance and the student's t test. A value of p<0.05 was considered statistically significant.

Example 1

This example describes the development of destination vectors for the one-step construction of adenovirus (OSCA) system using GDA technology.

To develop a panel of adenoviral vectors that can serve as common recipients for GDA reactions, three of the first-generation adenoviral shuttle vectors of the AdEasy system (12,13) were modified (i.e., pShuttle-CMV, pAdTrack-CMV and pAdTrace-CMV), by inserting an oligo cassette that contains a SwaI site flanked by two unique 20-bp sequences, namely MOS1 and MOS2 (FIG. 1A, panel i), to generate pShuttle-MOS, pAdTrack-MOS, and pAdTrace-MOS vectors. These plasmids were linearized with PmeI and transformed into BJ5183/pAdEasyl bacterial cells for homologous recombination (FIG. 1A, panel b). The kanamycin-resistant clones were picked up and subsequently confirmed by PCR and sequencing, resulting in pAdOS, pAdGOS, and pAdROS vectors.

To reduce potential background in GDA reactions, the above vectors were further modified by inserting the suicide gene ccdB expression cassette flanked with SwaI sites through GDA reactions, and grown in DB3.1 bacterial cells, resulting in the OSCA destination/recipient vectors, pAdOSd, pAdGOSd and pAdROSd (FIG. 1A, panel iii). The vector maps and full-length sequences for pAdGOSd and pAdROSd are presented in FIG. 6 and FIG. 7 .

The practical use of the GDA-based one-step construction of adenovirus (OSCA) system for transgene expression is illustrated in FIG. 1B. Briefly, the MOS1 and MOS2-anchored primers were used to amplify the coding region of the gene of interest (GOI) (FIG. 1B, panel i). The resulting PCR fragment was gel purified, and mixed with the SwaI-linearized destination vector, such as pAdOSd, pAdGOSd or pAdROSd, for GDA reactions to generate the GOI-containing recombinant adenoviral plasmid, pAdOS-GOI (FIG. 1B, panel ii). This recombinant adenoviral plasmid was digested with PacI and then transfected into optimized adenovirus packaging cells, such as 293pTP and RAPA, as described (17,18), leading to robust adenovirus packaging and production in 5-7 days (FIG. 1B, panel iii). The initial adenoviral lysate can be further amplified in HEK-293, 293pTP or RAPA cells to attain high titers for in vitro or in vivo use.

Example 2

This example demonstrates the generation of a copGFP-expressing adenoviral vector using the system described herein.

To carry out a proof-of-principle experiment, we the OSCA system described herein was used to make an adenoviral vector expressing the marker gene copGFP. The coding sequence of copGFP was amplified with MOS1 and MOS2 anchored primers, and the amplified fragment was purified (FIG. 2A, panels i & ii), yielding adenoviral plasmid pAdOS-copGFP.

Using the NEBUILDER® HiFi DNA Assembly kit, it was found that the GDA reactions were in general very efficient as ˜10% of the assembly products yielded nearly thousands of colonies after direct plating (FIG. 2B). PCR screening of randomly picked up clones indicated that 15 of 16 were positive for the presence of copGFP transgene (FIG. 2C). To further verify the structural integrity of adenoviral genome of the pAdOS-copGFP plasmids generated from the Gibson Assembly reactions, we digested the representative clones, in comparison with the adenoviral backbone vector pAdEasyl, with four restriction enzymes, Hind III (FIG. 2D, panel i), Kpn I (FIG. 2D, panel b), Barn HI (FIG. 2D, panel c), and Sph I (FIG. 2D, panel iv). The restriction digestion results indicated that all three selected clones yielded the same and expected digestion patterns (FIG. 2D). The assembled junctions were further verified by DNA sequencing. Collectively, these results demonstrate that the OSCA system is effective for GDA-based rapid construction of recombinant adenovirus plasmids.

It was next tested whether the pAdOS-copGFP plasmid could be effectively packaged into adenovirus. The pAdOS-copGFP plasmid was first linearized with PacI restriction enzyme, and then transfected into 293pTP cells (or RAPA cells, data not shown). While the transfection efficiency was modest, the GFP signal became increasingly intensified, and formed comet-like foci at 4 days after transfection, becoming apparent at day 7, which was also the endpoint of the adenovirus packaging (FIG. 3A). When the viral lysate was prepared at 7 days after transfection, HEK-293 cells were infected with different titers (as measured by % of the collected viral lysate) and demonstrated that significant copGFP expression was observed in a dose-dependent manner and was detected at levels as low as 0.1% of viral lysate (FIG. 3B, panels a-d).

These results indicate that the adenovirus production system described herein is highly efficient for construction of recombinant adenoviruses.

Example 3

This example demonstrates the high osteogenic activity of mouse BMP9 expressed by an adenoviral vector generated using the system described herein.

The biological functionality of OSCA-produced adenovirus was demonstrated by constructing the adenoviral vector AdROS-mBMP9 to express mouse BMP9 (mBMP9). Human BMP9 is one of the most osteogenic factors in promoting bone formation from mesenchymal stem cells (MSCs) (42-45). However, virtually no studies have been carried out to investigate the osteogenic activity of mouse BMP9 (mBMP9). Here, the coding region of mBMP9 was amplified with MOS1 and MOS2 anchored primers, and the adenoviral vector pAdROS-mBMP9 was generated using the OSCA system (FIG. 4A).

Consistent with the results shown in FIG. 2B-2D, the GDA reactions were effective and generated a high percentage of positive clones (FIG. 4B). Furthermore, the Pac linearized pAdROS-mBMP9 was shown to generate adenovirus with high efficiency in packaging cells (FIG. 4C and FIG. 8B). The generated AdROS-mBMP9 virus was shown to effectively transduce imBMSC MSCs in a titer-dependent fashion (FIG. 4D).

To test the biological function of mouse BMP9, the imBMSCs were infected with AdROSmBMP9 and control Ad-RFP viruses. mBMP9 effectively induced alkaline phosphatase (ALP) activities in a time-course dependent fashion, compared with that of the control Ad-RFP group (FIG. 5A), indicating that adenovirus-mediated expression of mouse BMP9 was able to induce early osteogenic marker ALP in MSCs. Furthermore, the adenovirus-mediated mouse BMP9 expression was shown to induce matrix mineralization (FIG. 5B). When the MSCs were infected with AdROS-mBMP9 or Ad-RFP (FIG. 5C, panel i), collected and injected subcutaneously into the athymic nude mice, robust bone formation was detected in the mBMP9 group, but not in the RFP control group, at 4 weeks after implantation as assessed by H & E staining (FIG. 5C, panel ii). Trichrome staining further revealed that mouse BMP9 induced robust trabecular bone formation with highly mineralized bone matrix (FIG. 5C, panel iii). Collectively, these results demonstrate that mBMP9 can be included in an adenoviral vector produced as described herein, and the resultant adenovirus can effectively transduce MSCs to induce osteogenic differentiation.

Sequences Nucleic acid sequence of the pAdGOSd vector (SEQ ID NO: 11). nnttaattaaggatccnnncctgtcctcgaccgatgcccttgagagccttcaacccagtcagctccttccg gtgggcgcggggcatgactatcgtcgccgcacttatgactgtc ttctttatcatgcaactcgtaggacaggtgccggcagcgctctgggtcattttcggcga ggaccgctttcgctggagcgcgacgatgatcggcctgtcgcttgcggtattcgga atcttgcacgccctcgctcaagccttcgtcactggtcccgccaccaaacgtttcggcgagaa gcaggccattatcgccggcatggcggccgacgcgctgggctacgtcttgc tggcgttcgcgacgcgaggctggatggccttccccattatgattcttctcgct tccggcggcatcgggatgcccgcgttgcaggccatgctgtccaggcaggtagatgacgac catcagggacagcttcaaggatcgctcgcggctcttaccagcctaacttcgatcactgg accgctgatcgtcacggcgatttatgccgcctcggcgagcacatggaacgggtt ggcatggattgtaggcgccgccctataccttgtctgcctccccgcgttgcgtcgcgg tgcatggagccgggccacctcgacctgaatggaagccggcggcacctcgctaac ggattcaccactccaagaattggagccaatcaattcttgcggagaactgtgaatgcgcaaaccaacccttggc agaacatatccatcgcgtccgccatctccagcagccgca cgcggcgcatctcgggcagcgttgggtcctggccacgggtgcgcatgatcgtgctcct gtcgttgaggacccggctaggctggcggggttgccttactggttagcagaatg aatcaccgatacgcgagcgaacgtgaagcgactgctgctgcaaaacgtctgcgacctgagcaacaa catgaatggtcttcggtttccgtgtttcgtaaagtctggaaacgcgg aagtcagcgccctgcaccattatgttccggatctgcatcgcaggatgctgctggctacc ctgtggaacacctacatctgtattaacgaagcgctggcattgaccctgagtgatttt tctctggtcccgccgcatccataccgccagttgtttaccctcacaacgttccagtaaccgggcat gttcatcatcagtaacccgtatcgtgagcatcctctctcgtttcatcggta tcattacccccatgaacagaaattcccccttacacggaggcatcaagtgaccaaacaggaaa aaaccgcccttaacatggcccgctttatcagaagccagacattaacgcttctg gagaaactcaacgagctggacgcggatgaacaggcagacatctgtgaatcgcttcacgacca cgctgatgagctttaccgcagctgcctcgcgcgtttcggtgatgacggt gaaaacctctgacacatgcagctcccggagacggtcacagcttgtctgtaagcggatgccggg agcagacaagcccgtcagggcgcgtcagcgggtgttggcgggtgtc ggggcgcagccatgacccagtcacgtagcgatagcggagtgtatactggcttaactatgcggcatca gagcagattgtactgagagtgcaccatatgcggtgtgaaataccg cacagatgcgtaaggagaaaataccgcatcaggcgctcttccgcttcctcgctcactgactcgc tgcgctcggtcgttcggctgcggcgagcggtatcagctcactcaaagg cggtaatacggttatccacagaatcaggggataacgcaggaaagaacatgtgagcaaaaggccag caaaaggccaggaaccgtaaaaaggccgcgttgctggcgtttttc cataggctccgcccccctgacgagcatcacaaaaatcgacgctcaagtcagaggtggcg aaacccgacaggactataaagataccaggcgtttccccctggaagctccctc gtgcgctctcctgttccgaccctgccgcttaccggatacctgtccgcctttc tcccttcgggaagcgtggcgctttctcaatgctcacgctgtaggtatctcagttcggtgtaggtc gttcgctccaagctgggctgtgtgcacgaaccccccgttcagcccgaccgctgcgccttatccggta actatcgtcttgagtccaacccggtaagacacgacttatcgccact ggcagcagccactggtaacaggattagcagagcgaggtatgtaggcggtgctacaga gttcttgaagtggtggcctaactacggctacactagaaggacagtatttggtatct gcgctctgctgaagccagttaccttcggaaaaagagttggtagctcttgatccggcaaacaaaccaccg ctggtagcggtggtttttttgtttgcaagcagcagattacgcgca gaaaaaaaggatctcaagaagatcctttgatcttttctacggggtctgacgctcagtggaacgaaaa ctcacgttaagggattttggtcatgagattatcaaaaaggatcttcacc tagatccttttaaattaaaaatgaagttttaaatcaatctaaagtatatatgagtaaacttggtct gacagttaccaatgcttaatcagtgaggcacctatctcagcgatctgtctat ttcgttcatccatagttgcctgactccccgtcgtgtagataactacgatacgggagggcttacca tctggccccagtgctgcaatgataccgcgagacccacgctcaccggctcca gatttatcagcaataaaccagccagccggaagggccgagcgcagaagtggtcctgcaacttt atccgcctccatccagtctattaattgttgccgggaagctagagtaagtagt tcgccagttaatagtttgcgcaacgttgttgnnaaaaaggatcttcacctagatccttttc acgtagaaagccagtccgcagaaacggtgctgaccccggatgaatgtcagcta ctgggctatctggacaagggaaaacgcaagcgcaaagagaaagcaggtagcttgcagtggg cttacatggcgatagctagactgggcggttttatggacagcaagcgaac cggaattgccagctggggcgccctctggtaaggttgggaagccctgcaaagtaaactggatggct ttctcgccgccaaggatctgatggcgcaggggatcaagctctgatc aagagacaggatgaggatcgtttcgcatgattgaacaagatggattgcacgcaggttctcc ggccgcttgggtggagaggctattcggctatgactgggcacaacagacaat cggctgctctgatgccgccgtgttccggctgtcagcgcaggggcgcccggttctttttgtc aagaccgacctgtccggtgccctgaatgaactgcaagacgaggcagcgcg gctatcgtggctggccacgacgggcgttccttgcgcagctgtgctcgacgttgtcactgaagcggg aagggactggctgctattgggcgaagtgccggggcaggatctcct gtcatctcaccttgctcctgccgagaaagtatccatcatggctgatgcaatgcggcggctg catacgcttgatccggctacctgcccattcgaccaccaagcgaaacatcgcat cgagcgagcacgtactcggatggaagccggtcttgtcgatcaggatgatctggacgaagagcatc aggggctcgcgccagccgaactgttcgccaggctcaaggcgagc atgcccgacggcgaggatctcgtcgtgacccatggcgatgcctgcttgccgaatatcatggtgga aaatggccgcttttctggattcatcgactgtggccggctgggtgtggc ggaccgctatcaggacatagcgttggctacccgtgatattgctgaagagcttggcggcgaatg ggctgaccgcttcctcgtgctttacggtatcgccgctcccgattcgcagc gcatcgccttctatcgccttcttgacgagttcttctgaattttgttaaaatttttgttaaat cagctcattttttaaccaataggccgaaatcggcaacatcccttataaatcaaaag aatagaccgcgatagggttgagtgttgttccagtttggaacaagagtccactattaaagaa cgtggactccaacgtcaaagggcgaaaaaccgtctatcagggcgatggcccacta cgtgaaccatcacccaaatcaagttttttgcggtcgaggtgccgtaaagctctaaatcggaa ccctaaagggagcccccgatttagagcttgacggggaaagccggcgaac gtggcgagaaaggaagggaagaaagcgaaaggagcgggcgctagggcgctggcaagt gtagcggtcacgctgcgcgtaaccaccacacccgcgcgcttaatgcgcc gnnttaattaannnntcccttccagctctctgccccttttggattgaagccaatatgataatgaggg ggtggagtttgtgacgtggcgcggggcgtgggaacggggcgggtg acgtagtagtgtggcggaagtgtgatgttgcaagtgtggcggaacacatgtaagcgac ggatgtggcaaaagtgacgtttttggtgtgcgccggtgtacacaggaagtgaca attttcgcgcggttttaggcggatgttgtagtaaatttgggcgtaaccgagtaa gatttggccattttcgcgggaaaactgaataagaggaagtgaaatctgaataattttgtgttac tcatagcgcgtaannncgcgttaagatacattgatgagtttggacaaaccacaactag aatgcagtgaaaaaaatgctttatttgtgaaatttgtgatgctattgctttatttgtaacc attataagctgcaataaacaagttaacaacaacaattgcattcattttatgtttcagg ttcagggggaggtgtgggaggttttttaaagcaagtaaaacctctacaaatgtggtatgg ctgattatgatcagttatctagatccggtggatctgagtccggacttgtacagctcgtc catgccgagagtgatcccggcggcggtcacgaactccagcaggaccatgtgatc gcgcttctcgttggggtctttgctcagggcggactgggtgctcaggtagtggttgtcgg gcagcagcacggggccgtcgccgatgggggtgttctgctggtagtggtcggcg agctgcacgctgccgtcctcgatgttgtggcggatcttgaagttcaccttgatgccgttcttctgcttg tcggccatgatatagacgttgtggctgttgtagttgtactccagcttgtg ccccaggatgttgccgtcctccttgaagtcgatgcccttcagctcgatgcggttcaccagggtgtcgccc tcgaacttcacctcggcgcgggtcttgtagttgccgtcgtccttg aagaagatggtgcgctcctggacgtagccttcgggcatggcggacttgaagaagtcgtg ctgcttcatgtggtcggggtagcggctgaagcactgcacgccgtaggtcagg gtggtcacgagggtgggccagggcacgggcagcttgccggtggtgcagatgaacttcagggt cagcttgccgtaggtggcatcgccctcgccctcgccggacacgctga acttgtggccgtttacgtcgccgtccagctcgaccaggatgggcaccaccccggtgaacagct cctcgcccttgctcaccatggtggcgaccggtagcgctagcggatctga cggttcactaaaccagctctgcttatatagacctcccaccgtacacgcctaccgcccatttgc gtcaatggggcggagttgttacgacattttggaaagtcccgttgattttggtgc caaaacaaactcccattgacgtcaatggggtggagacttggaaatccccgtgagtc aaaccgctatccacgcccattgatgtactgccaaaaccgcatcaccatggtaatagc gatgactaatacgtagatgtactgccaagtaggaaagtcccataaggtcatgtactg ggcataatgccaggcgggccatttaccgtcattgacgtcaatagggggcgtacttg gcatatgatacacttgatgtactgccaagtgggcagtttaccgtaaatactccacccattgacgt caatggaaagtccctattggcgttactatgggaacatacgtcattattgacg tcaatgggcgggggtcgttgggcggtcagccaggcgggccatttaccgtaagttatgtaa cgcggaactccatatatgggctatgaactaatgaccccgtaattgattactatta nnnctagcagatcctggttctttccgcctcagaagccatagagcccaccgcatccccagcatgcctg ctattgtcttcccaatcctcccccttgctgtcctgccccaccccaccc cccagaatagaatgacacctactcagacaatgcgatgcaatttcctcattttatta ggaaaggacagtgggagtggcaccttccagggtcaaggaaggcacgggggagggg caaacaacagatggctggcaactagaaggcacagtcgaggctgatcagcgggtttagcgg ccgatatcatttaaattgatttttgcggtataagaatatatactgatatgtatacc cgaagtatgtcaaaaagaggtatgctatgaagcagcgtattacagtgacagttgacagcgac agctatcagttgctcaaggcatatatgatgtcaatatctccggtctggtaagc acaaccatgcagaatgaagcccgtcgtctgcgtgccgaacgctggaaagcggaaaatcagg aagggatggctgaggtcgcccggtttattgaaatgaacggctcttttgctg acgagaacaggggctggtgaaatgcagtttaaggtttacacctataaaagagagagccgtta tcgtctgtttgtggatgtacagagtgatattattgacacgcccgggcgacgg atggtgatccccctggccagtgcacgtctgctgtcagataaagtctcccgtgaactttacccggtggtgcatatcgggga tgaaagctggcgcatgatgaccaccgatatggccagtgtgccggtctccgttatcggggaagaagtggctgatctcagc caccgcgaaaatgacatcaaaaacgccattaacctgatgttctggggaatataaatgtcaggctccct tatacacagccagtctgcagctcgctcttcatttaaatcctgaattcggtgtcttctatggaggtcaaaacagc gtggatggcgtctccaggcgatctgacggttcactaaacagc tcgatctctatcactgatagggagatctctatcactgatagggagatctctatcactgataggga gatctctatcactgatagggagagctctgcttatatagacctcccaccgtac acgcctaccgcccatttgcgtcaatggggcggagttgttacgacattttggaaagtcccgttgattttggttcca aaacaaactcccattgacgtcaatggggtggagacttgga aatccccgtgagtcaaaccgctatccacgcccattgatgtactgccaaaaccgcatcaccatggtaatagcga tgactaatacgtagatgtactgccaagtaggaaagtcccat aaggtcatgtactgggcataatgccaggcgggccatttaccgtcattgacgtcaataggg ggcgtacttggcatatgatacacttgatgtactgccaagtgggcagtttaccgta aatactccacccattgacgtcaatggaaagtccctattggcgttactatgggaacatacgtcattattgacgtcaat gggcgggggtcgttgggcggtcagccaggcgggcca tttaccgtaagttatgtaacgcggaactccatatatgggctatgaactaatgaccccgtaattgattac tattaataactagagnnnntaagggtgggaaagaatatataaggtgg gggtcttatgtagttttgtatctgttttgcagcagccgccgccgccatgagcaccaactcgtttgatggaag cattgtgagctcatatttgacaacgcgcatgcccccatgggccg gggtgcgtcagaatgtgatgggctccagcattgatggtcgccccgtcctgcccgcaaactct actaccttgacctacgagaccgtgtctggaacgccgttggagactgcagc ctccgccgccgcttcagccgctgcagccaccgcccgcg ggattgtgactgactttgctttcctgagcccgcttgcaagcagtgcagcttcccgttcatccgcccgcgatgaca agttgacggctcttttggcacaattggattctttgacccgggaacttaatgtcgtttctcagcagctgttggat ctgcgccagcaggtttctgccctgaaggcttcctcccctcccaa tgcggtttaaaacataaataaaaaaccagactctgtttggatttggatcaagcaagtgtcttgctgtctt tatttaggggttttgcgcgcgcggtaggcccgggaccagcggtctc ggtcgttgagggtcctgtgtattttttccaggacgtggtaaaggtgactctggatgttcagatacatgg gcataagcccgtctctggggtggaggtagcaccactgcagagcttc atgctgcggggtggtgttgtagatgatccagtcgtagcaggagcgctgggcgtggtgcctaaaaatgtcttt cagtagcaagctgattgccaggggcaggcccttggtgtaag tgtttacaaagcggttaagctgggatgggtgcatacgtggggatatgagatgcatcttgg actgtatttttaggttggctatgttcccagccatatccctccggggattcatgttgtg cagaaccaccagcacagtgtatccggtgcacttgggaaatttgtcatgtagcttagaag gaaatgcgtggaagaacttggagacgcccttgtgacctccaagattttccatgca ttcgtccataatgatggcaatgggcccacgggcggcggcctgggcgaagat atttctgggatcactaacgtcatagttgtgttccaggatgagatcgtcataggccatttttaca aagcgcgggcggagggtgccagactgcggtataatggttccatccggcccaggggc gtagttaccctcacagatttgcatttcccacgctttgagttcagatggggggatcat gtctacctgcggggcgatgaagaaaacggtttccggggtaggggagatcagctgggaa gaaagcaggttcctgagcagctgcgacttaccgcagccggtgggcccgtaa atcacacctattaccgggtgcaactggtagttaagagagctgcagctgc cgtcatccctgagcaggggggccacttcgttaagcatgtccctgactcgcatgttttccctgacc aaatccgccagaaggcgctcgccgcccagcgatagcagttcttgcaagg aagcaaagtttttcaacggtttgagaccgtccgccgtaggcatgcttttgagcgtttgaccaag cagttccaggcggtcccacagctcggtcacctgctctacggcatctcgatccagcat atctcctcgtttcgcgggttggggcggctttcgctgtacggcagtagtcggtgctcg tccagacgggccagggtcatgtctttccacgggcgcagggtcctcgtcagcgtagtctgggtcacggt gaaggggtgcgctccgggctgcgcgctggccagggtgcgctt gaggctggtcctgctggtgctgaagcgctgccggtcttcgccctgcgcgtcggccagg tagcatttgaccatggtgtcatagtccagcccctccgcggcgtggcccttggcg cgcagcttgcccttggaggaggcgccgcacgaggggcagtgcagacttttgagggcgtag agcttgggcgcgagaaataccgattccggggagtaggcatccgcgccg caggccccgcagacggtctcgcattccacgagccaggtgagctctggccgttcggggtc aaaaaccaggtttcccccatgctttttgatgcgtttcttacctctggtttccatga gccggtgtccacgctcggtgacgaaaaggctgtccgtgtccccgtatacagacttgagaggcc tgtcctcgagcggtgttccgcggtcctcctcgtatagaaactcggacca ctctgagacaaaggctcgcgtccaggccagcacgaaggaggctaagtgggaggggtagcgg tcgttgtccactagggggtccactcgctccagggtgtgaagacacatg tcgccctcttcggcatcaaggaaggtgattggtttgtaggtgtaggccacgtgaccgggtg ttcctgaaggggggctataaaagggggtgggggcgcgttcgtcctcactctc ttccgcatcgctgtctgcgagggccagctgttggggtgagtactccctctgaaaagcgggca tgacttctgcgctaagattgtcagtttccaaaaacgaggaggatttgatattc acctggcccgcggtgatgcctttgagggtggccgcatccatctggtcagaaaagacaatctttt tgttgtcaagcttggtggcaaacgacccgtagagggcgttggacagcaa cttggcgatggagcgcagggtttggtttttgtcgcgatcggcgcgctccttggccgcg atgtttagctgcacgtattcgcgcgcaacgcaccgccattcgggaaagacggtgg tgcgctcgtcgggcaccaggtgcacgcgccaaccgcggttgtgcagggtgacaaggtcaacgctgg tggctacctctccgcgtaggcgctcgttggtccagcagaggcg gccgcccttgcgcgagcagaatggcggtagggggtctagctgcgtctcgtccggggggtctgcgtc cacggtaaagaccccgggcagcaggcgcgcgtcgaagtagtct atcttgcatccttgcaagtctagcgcctgctgccatgcgcgggcggcaagcgcgcgctcgtat gggttgagtgggggaccccatggcatggggtgggtgagcgcggaggc gtacatgccgcaaatgtcgtaaacgtagaggggctctctgagtattccaagatatgtagggtagca tcttccaccgcggatgctggcgcgcacgtaatcgtatagttcgtgcga gggagcgaggaggtcgggaccgaggttgctacgggcgggctgctctgctcggaagactatc tgcctgaagatggcatgtgagttggatgatatggttggacgctggaaga cgttgaagctggcgtctgtgagacctaccgcgtcacgcacgaaggaggcgtaggagtcgcgcagcttg ttgaccagctcggcggtgacctgcacgtctagggcgcagtag tccagggtttccttgatgatgtcatacttatcctgtcccttttttttccacagctcgcggttga ggacaaactcttcgcggtctttccagtactcttggatcggaaacccgtcggc ctccgaacggtaagagcctagcatgtagaactggttgacggcctggtaggcgcagcatccc ttttctacgggtagcgcgtatgcctgcgcggccttccggagcgaggtgtgggt gagcgcaaaggtgtccctgaccatgactttgaggtactggtatttgaagtcagtgtcgtcg catccgccctgctcccagagcaaaaagtccgtgcgctttttggaacgcggattt ggcagggcgaaggtgacatcgttgaagagtatctttcccgcgcgaggcataaagttgcgtgtgatgcggaagggt cccggcacctcggaacggttgttaattacctgggcg gcgagcacgatctcgtcaaagccgttgatgttgtggcccacaatgtaaagttccaagaagcg cgggatgcccttgatggaaggcaattttttaagttcctcgtaggtgagctctt caggggagctgagcccgtgctctgaaagggcccagtctgcaagatgagggttggaagcgacgaatgagctcca caggtcacgggccattagcatttgcaggtggtcgcg aaaggtcctaaactggcgacctatggccattttttctggggtgatgcagtagaaggtaagcgggtcttgttcccagc ggtcccatccaaggttcgcggctaggtctcgcgcgg cagtcactagaggctcatctccgccgaacttcatgaccagcatgaagggcacgagctgcttcccaaaggcccccat ccaagtataggtctctacatcgtaggtgacaaagag acgctcggtgcgaggatgcgagccgatcgggaagaactggatctcccgccaccaattggaggagt ggctattgatgtggtgaaagtagaagtccctgcgacgggccgaac actcgtgctggcttttgtaaaaacgtgcgcagtactggcagcggtgcacgggctgtacatcctgcacgagg ttgacctgacgaccgcgcacaaggaagcagagtgggaattt gagcccctcgcctggcgggtttggctggtggtcttctacttcggctgcttgtccttgaccgtctggctgctcgag gggagttacggtggatcggaccaccacgccgcgcgagc ccaaagtccagatgtccgcgcgcggcggtcggagcttgatgacaacatcgcgcagatgggagctgtcca tggtctggagctcccgcggcgtcaggtcaggcgggagctc ctgcaggtttacctcgcatagacgggtcagggcgcgggctagatccaggtgatacctaatttccaggggctgg ttggtggcggcgtcgatggcttgcaagaggccgcatcc ccgcggcgcgactacggtaccgcgcggcgggcggtgggccgcgggggtgtccttggatgatgcatctaaaa gcggtgacgcgggcgagcccccggaggtagggggg gctccggacccgccgggagagggggcaggggcacgtcggcgccgcgcgcgggcaggagctggtgctgcgcgcgta ggttgctggcgaacgcgacgacgcggcggt tgatctcctgaatctggcgcctctgcgtgaagacgacgggcccggtgagcttgagcctgaaagagagttcg acagaatcaatttcggtgtcgttgacggcggcctggcgcaa aatctcctgcacgtctcctgagttgtcttgataggcgatctcggccatgaactgctcgatctcttcctcct ggagatctccgcgtccggctcgctccacggtggcggcgaggtcg ttggaaatgcgggccatgagctgcgagaaggcgttgaggcctccctcgttccagacgcggctgtagaccac gcccccttcggcatcgcgggcgcgcatgaccacctgcgc gagattgagctccacgtgccgggcgaagacggcgtagtttcgcaggcgctgaaagaggtagttgagggtgg tggcggtgtgttctgccacgaagaagtacataacccagc gtcgcaacgtggattcgttgatatcccccaaggcctcaaggcgctccatggcctcgtagaagtccacggcgaag ttgaaaaactgggagttgcgcgccgacacggttaactc ctcctccagaagacggatgagctcggcgacagtgtcgcgcacctcgcgctcaaaggctacaggggc ctcttcttcttcttcaatctcctcttccataagggcctccccttcttctt cttctggcggcggtgggggaggggggacacggcggcgacgacggcgcaccgggaggcggtcgacaaagcg ctcgatcatctccccgcggcgacggcgcatggtctc ggtgacggcgcggccgttctcgcgggggcgcagttggaagacgccgcccgtcatgtcccggttatgggttggc ggggggctgccatgcggcagggatacggcgctaac gatgcatctcaacaattgttgtgtaggtactccgccgccgagggacctgagcgagtccgcatcg accggatcggaaaacctctcgagaaaggcgtctaaccagtcacagtc gcaaggtaggctgagcaccgtggcgggcggcagcgggcggcggtcggggttgtttctggcgg aggtgctgctgatgatgtaattaaagtaggcggtcttgagacggcgg atggtcgacagaagcaccatgtccttgggtccggcctgctgaatgcgcaggcggtcggccatgccccaggct tcgttttgacatcggcgcaggtctttgtagtagtcttgcatg agcctttctaccggcacttcttcttctccttcctcttgtcctgcatctcttgcatct atcgctgcggcggcggcggagtttggccgtaggtggcgccctcttcctcccatgcgtg tgaccccgaagcccctcatcggctgaagcagggctaggtcggcgacaacgcgctcggctaatatg gcctgctgcacctgcgtgagggtagactggaagtcatccatgtccaca aagcggtggtatgcgcccgtgttgatggtgtaagtgcagttggccataacggaccagttaacg gtctggtgacccggctgcgagagctcggtgtacctgagacgcgagtaa gccctcgagtcaaatacgtagtcgttgcaagtccgcaccaggtactggtatcccaccaaaaagtgcggc ggcggctggcggtagaggggccagcgtagggtggccgggg ctccgggggcgagatcttccaacataaggcgatgatatccgtagatgtacctggacatccaggtgatgccg gcggcggtggtggaggcgcgcggaaagtcgcggacgcg gttccagatgttgcgcagcggcaaaaagtgctccatggtcgggacgctctggccggtc aggcgcgcgcaatcgttgacgctctaccgtgcaaaaggagagcctgtaagcg ggcactcttccgtggtctggtggataaattcgcaagggtatcatggcggacgaccggggttc gagccccgtatccggccgtccgccgtgatccatgcggttaccgcccgcgt gtcgaacccaggtgtgcgacgtcagacaacgggggagtgctccttttggcttccttccaggcgcggcggctg ctgcgctagcttttttggccactggccgcgcgcagcgtaa gcggttaggctggaaagcgaaagcattaagtggctcgctccctgtagccggagggttattttccaagggt tgagtcgcgggacccccggttcgagtctcggaccggccgga ctgcggcgaacgggggtttgcctccccgtcatgcaagaccccgcttgcaaattcctccggaaacagggacg agccccttttttgcttttcccagatgcatccggtgctgcggc agatgcgcccccctcctcagcagcggcaagagcaagagcagcggcagacatgcagggcaccctcccctcct cctaccgcgtcaggaggggcgacatccgcggttgacg cggcagcagatggtgattacgaacccccgcggcgccgggcccggcactac ctggacttggaggagggcgagggcctggcgcggctaggagcgccctctcctgagcgg tacccaagggtgcagctgaagcgtgatacgcgtgaggcgtacgtgccgcggcagaacctgtttcgcgaccgcg agggagaggagcccgaggagatgcgggatcgaaa gttccacgcagggcgcgagctgcggcatggcctgaatcgcgagcggttgctgcgcgagga ggactttgagcccgacgcgcgaaccgggattagtcccgcgcgcgcaca cgtggcggccgccgacctggtaaccgcatacgagcagacggtgaaccaggagattaactttcaaa aaagctttaacaaccacgtgcgtacgcttgtggcgcgcgaggagg tggctataggactgatgcatctgtgggactttgtaagcgcgctggagcaaaacccaaatagcaagccgct catggcgcagctgttccttatagtgcagcacagcagggacaa cgaggcattcagggatgcgctgctaaacatagtagagcccgagggccgctggctgctcgat ttgataaacatcctgcagagcatagtggtgcaggagcgcagcttgagcct ggctgacaaggtggccgccatcaactattccatgcttagcctgggcaagttttacgcccgcaagatataccata ccccttacgttcccatagacaaggaggtaaagatcgagg ggttctacatgcgcatggcgctgaaggtgcttaccttgagcgacgacctgggcgtttatcgcaa cgagcgcatccacaaggccgtgagcgtgagccggcggcgcgagctc agcgaccgcgagctgatgcacagcctgcaaagggccctggctggcacgggcagcggcgatagagaggccga gtcctactttgacgcgggcgctgacctgcgctgggc cccaagccgacgcgccctggaggcagctggggccggacctgggctggcggtggcacccgcgcgcgctggc aacgtcggcggcgtggaggaatatgacgaggacgat gagtacgagccagaggacggcgagtactaagcggtgatgtttctgatcagatgatgcaagacgcaacggacccggcggtg cgggcggcgctgcagagccagccgtccggccttaactccacggacgactggcgccaggtc atggaccgcatcatgtcgctgactgcgcgcaatcctgacgcgttccggcagcagccgcaggccaaccggctctccgca attctggaagcggtggtcccggcgcgcgcaaaccccacgcacgagaaggtgctggcgatcgt aaacgcgctggccgaaaacagggccatccggcccgacgaggccgg cctggtctacgacgcgctgcttcagcgcgtggctcgttacaacagcggcaacgtgcag accaacctggaccggctggtgggggatgtgcgcgaggccgtggcgcagcgt gagcgcgcgcagcagcagggcaacctgggctccatggttgcactaaacgccttcctgagtac acagcccgccaacgtgccgcggggacaggaggactacaccaactttg tgagcgcactgcggctaatggtgactgagacaccgcaaagtgaggtgtaccagtctgggccagactattt tttccagaccagtagacaaggcctgcagaccgtaaacctgagccaggctttcaaaaacttgcaggggctgtgg ggggtgcgggctcccacaggcgaccgcgcgaccgtgtctagcttgctgacgcccaactcgcgcctgttgctgctgctaata gcgcccttcacggacagtggcagcgtgtcccgggacacatacctaggtcacttgctgacactgtaccgcgaggccata ggtcaggcgcatgtggacgagcatactttccag gagattacaagtgtcagccgcgcgctggggcaggaggacacgggcagcctggaggcaaccct aaactacctgctgaccaaccggcggcagaagatcccctcgttgcac agtttaaacagcgaggaggagcgcattttgcgctacgtgcagcagagcgtgagccttaacc tgatgcgcgacggggtaacgcccagcgtggcgctggacatgaccgcgc gcaacatggaaccgggcatgtatgcctcaaaccggccgtttatcaaccgcctaatggactacttg catcgcgcggccgccgtgaaccccgagtatttcaccaatgccatcttg aacccgcactggctaccgccccctggtttctacaccgggggattcgaggtgcccgagggtaacgatg gattcctctgggacgacatagacgacagcgtgttttccccgcaac cgcagaccctgctagagttgcaacagcgcgagcaggcagaggcggcgctgcgaaaggaaagcttccgcaggcc aagcagcttgtccgatctaggcgctgcggccccgc ggtcagatgctagtagcccatttccaagcttgatagggtctcttaccagcactcgcaccacccgcccgcgc ctgctgggcgaggaggagtacctaaacaactcgctgctgca gccgcagcgcgaaaaaaacctgcctccggcatttcccaacaacgggatagagagcctagtggacaagatgagtag atggaagacgtacgcgcaggagcacagggacgt gccaggcccgcgcccgcccacccgtcgtcaaaggcacgaccgtcagcggggtctggtgtgggaggacga tgactcggcagacgacagcagcgtcctggatttgggagggagtggcaacccgtttgcgcaccttcgcccc aggctggggagaatgttttaaaaaaaaaaaagcatgatgcaaaataaaaaactcaccaaggccatggcaccgagcgttg gttttcttgtattccccttagtatgcggcgcgcggcgatgtatgaggaaggtcctcctccctcctacgagag tgtggtgagcgcggcgccagtggcggcggcgctgggttctc ccttcgatgctcccctggacccgccgtttgtgcctccgcggtacctgcggcctaccgggggg agaaacagcatccgttactctgagttggcacccctattcgacaccacccgt gtgtacctggtggacaacaagtcaacggatgtggcatccctgaactaccagaacgacca cagcaactttctgaccacggtcattcaaaacaatgactacagcccgggggag gcaagcacacagaccatcaatcttgacgaccggtcgcactggggcggcgacctgaaaac catcctgcataccaacatgccaaatgtgaacgagttcatgtttaccaataagtt taaggcgcgggtgatggtgtcgcgcttgcctactaaggacaatcaggtggagctgaaata cgagtgggtggagttcacgctgcccgagggcaactactccgagaccatga ccatagaccttatgaacaacgcgatcgtggagcactacttgaaagtgggcagacagaacggggttctggaaagcg acatcggggtaaagtttgacacccgcaacttcagac tggggtttgaccccgtcactggtcttgtcatgcctggggtatatacaaacgaagccttccatccagacatcattttg ctgccaggatgcggggtggacttcacccacagccgcct gagcaacttgttgggcatccgcaagcggcaacccttccaggagggctttaggatcacctacgatgatct ggagggtggtaacattcccgcactgttggatgtggacgcctacc aggcgagcttgaaagatgacaccgaacagggcgggggtggcgcaggcggcagcaacagcagtggcagcgg cgcggaagagaactccaacgcggcagccgcggca atgcagccggtggaggacatgaacgatcatgccattcgcggcgacacc tttgccacacgggctgaggagaagcgcgctgaggccgaagcagcggccgaagctgccgc ccccgctgcgcaacccgaggtcgagaagcctcagaagaaaccggtgatcaaacccctgacagaggacagc aagaaacgcagttacaacctaataagcaatgacagcac cttcacccagtaccgcagctggtaccttgcatacaactacggcgaccctcagaccggaatccgctcatggaccctgc tttgcactcctgacgtaacctgcggctcggagcag gtctactggtcgttgccagacatgatgcaagaccccgtgaccttccgctccacgcgccagatcagcaactttccggt ggtgggcgccgagctgttgcccgtgcactccaaga gcttctacaacgaccaggccgtctactcccaactcatccgccagtttacctctctgacccacgtgttcaa tcgctttcccgagaaccagattttggcgcgcccgccagccccca ccatcaccaccgtcagtgaaaacgttcctgctctcacagatcacgggacgctaccgctgcgcaacagcatcgg aggagtccagcgagtgaccattactgacgccagacgc cgcacctgcccctacgtttacaaggccctgggcatagtctcgccgcgcgtcctatcgagccgcacttt ttgagcaagcatgtccatccttatatcgcccagcaataacacaggc tggggcctgcgcttcccaagcaagatgtttggcggggccaagaagcgctccgaccaacacccagtgcgcgtgcgcgggc actaccgcgcgccctggggcgcgcacaaacgcggccgcactgggcgcaccaccgtcgatgacgc catcgacgcggtggtggaggaggcgcgcaactacacgcccacgccgccaccagtgtccacagtggacgcgg ccattcagaccgtggtgcgcggagcccggcgctatgctaaaatgaagagacggcggaggcgcgtagcacgt cgccaccgccgccgacccggcactgccgcccaacgc gcggcggcggccctgcttaaccgcgcacgtcgcaccggccgacgggcggccatgcgggccgctc gaaggctggccgcgggtattgtcactgtgccccccaggtccag gcgacgagcggccgccgcagcagccgcggccattagtgctatgactcagggtcgcaggggcaacgtgtattg ggtgcgcgactcggttagcggcctgcgcgtgcccgtgcgcacccgccccccgcgcaactagattgcaagaaa aaactacttagactcgtactgttgtatgtatccagcggcggcggcgcgcaacgaagctatgtccaagcgcaaaatc aaagaagagatgctccaggtcatcgcgccggagatctatggccccccgaagaaggaagagcagg attacaagccccgaaagctaaagcgggtcaaaaagaaaaagaaa gatgatgatgatgaacttgacgacgaggtggaactgctgcacgctaccgcgcccaggcgacgggtacag tggaaaggtcgacgcgtaaaacgtgttttgcgacccggcac caccgtagtctttacgcccggtgagcgctccacccgcacctacaagcgcgtgtatgatgaggtgtacggcgacg aggacctgcttgagcaggccaacgagcgcctcgggg agtttgcctacggaaagcggcataaggacatgctggcgttgccgctggacgagggcaacccaac acctagcctaaagcccgtaacactgcagcaggtgctgcccgcgctt gcaccgtccgaagaaaagcgcggcctaaagcgcgagtctggtgacttggcacccaccgtgc agctgatggtacccaagcgccagcgactggaagatgtcttggaaaaaat gaccgtggaacctgggctggagcccgaggtccgcgtgcggccaatcaagcaggtggcgccgggactgggcgt gcagaccgtggacgttcagatacccactaccagtag caccagtattgccaccgccacagagggcatggagacacaaacgtccccggttgcctcag cggtggcggatgccgcggtgcaggcggtcgctgcggccgcgtccaagac ctctacggaggtgcaaacggacccgtggatgtttcgcgtttcagccccccggcgcccgcgcggt tcgaggaagtacggcgccgccagcgcgctactgcccgaatatgccc tacatccttccattgcgcctacccccggctatcgtggctacacctaccgccccagaagacga gcaactacccgacgccgaaccaccactggaacccgccgccgccgtcgc cgtcgccagcccgtgctggccccgatttccgtgcgcagggtggctcgcgaaggaggcaggacc ctggtgctgccaacagcgcgctaccaccccagcatcgtttaaaagc cggtctttgtggttcttgcagatatggccctcacctgccgcctccgtttcccggtgccggga ttccgaggaagaatgcaccgtaggaggggcatggccggccacggcctgac gggcggcatgcgtcgtgcgcaccaccggcggcggcgcgcgtcgcaccgtcgcatgcgcggcggta tcctgcccctccttattccactgatcgccgcggcgattggcgcc gtgcccggaattgcatccgtggccttgcaggcgcagagacactgattaaaaacaagttgcatgtggaaaaatcaaa ataaaaagtctggactctcacgctcgcttggtcctgta actattttgtagaatggaagacatcaactttgcgtctctggccccgcgacacggctcgcgcccgttcatgggaaa ctggcaagatatcggcaccagcaatatgagcggtggc gccttcagctggggctcgctgtggagcggcattaaaaatttcggttccaccgttaagaactatggcagcaag gcctggaacagcagcacaggccagatgctgagggataag ttgaaagagcaaaatttccaacaaaaggtggtagatggcctggcctctggcattagcggggtggtggacctggccaac caggcagtgcaaaataagattaacagtaagcttg atccccgccctcccgtagaggagcctccaccggccgtggagacagtgtctccagaggggcgtggcg aaaagcgtccgcgccccgacagggaagaaactctggtgacgc aaatagacgagcctccctcgtacgaggaggcactaaagcaaggcctgcccaccacccgtcccatcgcgccc atggctaccggagtgctgggccagcacacacccgtaac gctggacctgcctccccccgccgacacccagcagaaacctgtgctgccaggcccgaccgccgttgttgtaaccc gtcctagccgcgcgtccctgcgccgcgccgccagcggtccgcgatcgttgcggcccgtagccagtggcaactggc aaagcacactgaacagcatcgtgggtctgggggtgcaatccctgaagcgccgacgatgcttctgaatagct aacgtgtcgtatgtgtgtcatgtatgcgtccatgtcgccgccagaggagctgctgagccgccgcgcgcccgctttccaag atggctaccccttcgatgatgccgcagtggtctt acatgcacatctcgggccaggacgcctcggagtacctgagccccgggctggtgcagtttg cccgcgccaccgagacgtacttcagcctgaataacaagtttagaaacccca cggtggcgcctacgcacgacgtgaccacagaccggtcccagcgtttgacgctgcggttcatccctgtgg accgtgaggatactgcgtactcgtacaaggcgcggttcaccctagctgtgggtgataaccgtgtgctggacatggcttcc acgtactttgacatccgcggcgtgctggacaggggccctacttttaagccctactctggcactgcctacaacgccc tggctcccaagggtgccccaaatccttgcgaatgggatgaagctgctactgctcttga aataaacctagaagaagaggacgatgacaacgaagacgaagtagacgagcaa gctgagcagcaaaaaactcacgtatttgggcaggcgccttattctggtataaatattacaaaggag ggtattcaaataggtgtcgaaggtcaaacacctaaatatgccgataaaacatttcaacctgaacctcaaataggagaa tctcagtggtacgaaactgaaattaatcatgcagctgggagagtccttaaaaagactaccccaatgaaaccatgttacggttcat atgcaaaacccacaaatgaaaatggagggcaaggcattcttgtaaagcaacaaaatggaaagctagaaagtcaagtggaaatg caatttttctcaactactgaggcgaccgc aggcaatggtgataacttgactcctaaagtggtattgtacagtgaagatgtagatatagaaaccccagacactcatatttcttaca tgcccactattaaggaaggtaactcacgagaactaatgggccaacaatctatgcccaacaggcctaattacattgcttttaggga caattttattggtctaatgtattacaacagcacgggtaatatgggtgttctggcgggccaagcatcgcagttgaatgctgttgtag atttgcaagacagaaacacagagct ttcataccagcttttgcttgattccattggtgatagaaccaggtacttttctatgtggaatcaggctgtt gacagctatgatccagatgttagaattattgaaaatcatggaactgaagatgaacttccaaattactgctttccactg ggaggtgtgattaatacagagactcttaccaaggtaaaacctaaaacaggtcaggaaaatggatgggaaaaagat gctacagaattttcagataaaaatgaaataagagttggaaataattttgccatggaaatcaatctaaatgccaacctgt ggagaaatttcctgtactccaacatagcgctgtatttgcccgacaagctaaagtacagtccttccaacgtaaaaatttctga taacccaaacacctacgactacatgaacaagcg agtggtggctcccgggttagtggactgctacattaaccttggagcacgctggtcccttgactatatggaca acgtcaacccatttaaccaccaccgcaatgctggcctgcgctaccgctcaatgttgctgggcaatggtcgctat gtgcccttccacatccaggtgcctcagaagttctttgccattaaaaacctccttctcctgccgggctcatacacctacgagtgga acttcaggaaggatgttaacatggttctgcagagctccctaggaaatgacctaagggttgacggagccagcatt aagtttgatagcatttgcctttacgccaccttcttccccatg gcccacaacaccgcctccacgcttgaggccatgcttagaaacgacaccaacgaccagtcctttaacgactatct ctccgccgccaacatgctctaccctatacccgccaacg ctaccaacgtgcccatatccatcccctcccgcaactgggcggctttccgcggctgggccttcacgcgccttaagactaag gaaaccccatcactgggctcgggctacgaccc ttattacacctactctggctctataccctacctagatggaaccttttacctcaaccacacctttaagaaggt ggccattacctttgactcttctgtcagctggcctggcaatgaccgcctgcttacccccaacgagtttgaaattaa gcgctcagttgacggggagggttacaacgttgcccagtgtaacatgaccaaagactggttcctggtacaaatgctagctaa ctacaacattggctaccagggcttctatatcccagagagctacaaggaccgcatgtactccttctttag aaacttccagcccatgagccgtcaggtggtggatgatactaaatacaag gactaccaacaggtgggcatcctacaccaacacaacaactctggatttgttggctaccttgcccccacca tgcgcgaaggacaggcctaccctgctaacttcccctatccgctt ataggcaagaccgcagttgacagcattacccagaaaaagtttctttgcgatcgcaccctttggcgcatccca ttctccagtaactttatgtccatgggcgcactcacagacctgg gccaaaaccttctctacgccaactccgcccacgcgctagacatgacttttgaggtggatcccatggacgagcccacccttct ttatgttttgtttgaagtctttgacgtggtccgtg tgcaccggccgcaccgcggcgtcatcgaaaccgtgtacctgcgcacgcccttctcggccggcaacgc cacaacataaagaagcaagcaacatcaacaacagctgccgcc atgggctccagtgagcaggaactgaaagccattgtcaaagatcttggttgtgggccatattttttgggcacctatgac aagcgctttccaggctttgtttctccacacaagctcgc ctgcgccatagtcaatacggccggtcgcgagactgggggcgtacactggatggcctt tgcctggaacccgcactcaaaaacatgctacctctttgagccctttggcttttctga ccagcgactcaagcaggtttaccagtttgagtacgagtcactcctgcgccgtagcgccattgcttcttcccccgaccgct gtataacgctggaaaagtccacccaaagcgtacaggggcccaactcggccgcctgtggactattctgctgcatgtt tctccacgcctttgccaactggccccaaactcccatggatcacaaccccaccatgaaccttattaccgggg tacccaactccatgctcaacagtccccaggtacagcccaccctgcgtcgcaaccaggaacagctctacagcttcctggagc gccactcgccctacttccgcagccacagtgc gcagattaggagcgccacttctttttgtcacttgaaaaacatgtaaaaataatgtactaga gacactttcaataaaggcaaatgcttttatttgtacactctcgggtgattattta cccccacccttgccgtctgcgccgtttaaaaatcaaaggggttctgccgcgcatcgctatgcgccactggcagggacacgt tgcgatactggtgtttagtgctccacttaaactcaggcacaaccatccgcggcagctcggtgaagttttcac tccacaggctgcgcaccatcaccaacgcgtttagcaggtcgggcgccgatatcttgaagtcgcagttggggcctccg ccctgcgcgcgcgagttgcgatacacagggttgcagcactggaacactatcagcgccgggtggtgcacgctggccag cacgctcttgtcggagatcagatccgcgtccaggtcctccgcgttgctcagggcgaacggagtcaactttggtagc tgccttcccaaaaagggcgcgtgcccaggctttgagttgcactcgcaccgtagtggcatcaaaaggtga ccgtgcccggtctgggcgttaggatacagcgcctgcataaaagccttgatctgcttaaaagccacctgagcctttgcgcc ttcagagaagaacatgccgcaagacttgccggaaaactgattggccggacaggccgcgtcgtgcacgcagcaccttgc gtcggtgttggagatctgcaccacatttcggccccaccggttcttcacgatcttggccttgctagact gctccttcagcgcgcgctgcccgttttcgctcgtcacatccatttcaatcacgtgctccttatttatcata atgcttccgtgtagacacttaagctcgccttcgatctcagcgca gcggtgcagccacaacgcgcagcccgtgggctcgtgatgcttgtaggtcacctctgcaaacgactgcaggtacgcctgcaggaat cgccccatcatcgtcacaaaggtcttgttgctggtgaaggtcagctgcaacccgcggtgctcctcgt tcagccaggtcttgcatacggccgccagagcttccacttggtcaggcagtagtttgaagttcgcctttagatcgttat ccacgtggtacttgtccatcagcgcgcgcgcagcctccatgcccttctcccacgcagacacgatcggcacactcagcgggttcat caccgtaatttcactttccgcttcgctgggctcttcctcttcctcttgcgtccgcataccacgcgccactgggtcgtcttcattca gccgccgcactgtgcgcttacctcctttgccatgcttgattagcaccggtgggttgctga aacccaccatttgtagcgccacatcttctctttcttcctcgctgtccacgattacctctggtgatggcgggcgctcgggctt gggagaagggcgcttctttttcttcttgggcgcaatggccaaatccgccgccgaggtc gatggccgcgggctgggtgtgcgcggcaccagcgcgtcttgtgatgagtcttcctcgtcctcggactcgatacgccgcctcatccgcttt tttgggggcgcccggggaggcggcggcgacggggacggggacgacacgtcctccatggttgg gggacgtcgcgccgcaccgcgtccgcgctcgggggtggtttcgcgctgctcctcttcccgactggccatttccttctccta taggcagaaaaagatcatggagtcagtcgagaagaaggacagcctaaccgccccctctgagttcgccaccaccgcctc caccgatgccgccaacgcgcctaccaccttccccgtcgaggcacccccgcttgaggaggaggaagtga ttatcgagcaggacccaggttttgtaagcgaagacgacgaggaccgctcagtaccaacagaggataaaaagcaagaccaggaca acgcagaggcaaacgaggaacaagtcgggcggggggacgaaaggcatggcgactacctagatg tgggagacgacgtgctgttgaagcatctgcagcgccagtgcgccattatctgcgacgcgttgcaagagcgcagc gatgtgcccctcgccatagcggatgtcagccttgcctacgaacgccacctattctcaccgcgcgtaccccccaaacg ccaagaaaacggcacatgcgagcccaacccgcgcctcaacttctaccccgtatttgccgtgccagaggtgct tgccacctatcacatctttttccaaaactgcaagatacccctatcctgccgtgccaaccgcagccgagcggacaagc agctggccttgcggcagggcgctgtcatacctgatatcgcctcgctcaacgaagtgccaaaaatctttgagggtctt ggacgcgacgagaagcgcgcggcaaacgctctgcaacaggaaaacagcgaaaatgaaagtcactctgga gtgttggtggaactcgagggtgacaacgcgcgcctagccgtactaaaacgcagcatcgaggtcacccactttgcctacccggc acttaacctaccccccaaggtcatgagcacagtcatgagtgagctgatcgtgcgccgtgcgcagcccctggagaggga tgcaaatttgcaagaacaaacagaggagggcctacccgcagttggcgacgagcagctag cgcgctggcttcaaacgcgcgagcctgccgacttggaggagcgacgcaaactaatgatggccgcagtgctcgttaccgtgga gcttgagtgcatgcagcggttctttgctgacccggagatgcagcgcaagctagaggaaacattg cactacacctttcgacagggctacgtacgccaggcctgcaagatctccaacgtggagctctgcaacctggtctccta ccttggaattttgcacgaaaaccgccttgggcaaaacgtgcttcattccacgctcaagggcgaggcgcgccgcgactacgtc cgcgactgcgtttacttatttctatgctacacctggcagacggccatgggcgtttggcagcagtgc ttggaggagtgcaacctcaaggagctgcagaaactgctaaagcaaaacttgaaggacctatggacggccttcaacga gcgctccgtggccgcgcacctggcggacatcattttccccgaacgcctgcttaaaaccctgcaacagggt ctgccagacttcaccagtcaaagcatgttgcagaactttagga actttatcctagagcgctcaggaatcttgcccgccacctgctgtgcacttcctagcgactttgtgcccattaagtaccg cgaatgccctccgccgctttggggccactgctaccttctgcagctagccaactaccttgcctaccact ctgacataatggaagacgtgagcggtgacggtctactggagtgtcactgtcgctgcaacctatgcaccccgcaccgctccct ggtttgcaattcgcagctgcttaacgaaagtcaaattatcggtacctttgagctgcagggtccctcgcctgacgaaaagtccgc ggctccggggttgaaactcactccggggctgtggacgtcggcttaccttcgca aatttgtacctgaggactaccacgcccacgagattaggttctacgaagaccaatcccgcccgccaaatgcggagctt accgcctgcgtcattacccagggccacattcttggccaattgcaagccatcaacaaagcccgc caagagtttctgctacgaaagggacggggggtttacttggacccccagtccggcgaggagc tcaacccaatccccccgccgccgcagccctatcagcagcagccgcgggcccttgcttcccaggatggcaccca aaaagaagctgcagctgccgccgccacccacggacgaggaggaatactgggacagtcaggcagaggaggttttg gacgaggaggaggaggacatgatggaagactgggagagcctagacgaggaagcttccgaggtcgaaga ggtgtcagacgaaacaccgtcaccctcggtcgcattcccctcgccggcgccccagaaatcggcaaccggttccagcatggc tacaacctccgctcctcaggcgccgccggcactgcccgttcgccgacccaaccgtagatgggacaccactggaacc agggccggtaagtccaagcagccgccgccgttagcccaagagcaacaacagcgccaaggct accgctcatggcgcgggcacaagaacgccatagttgcttgcttgcaagactgtgggggcaacatctc cttcgcccgccgctttcttctctaccatcacggcgtggccttcccccgtaacatcctgcattactaccgtcatctc tacagcccatactgcaccggcggcagcggcagcggcagcaacagcagcggccacacagaagcaaaggcgaccggatagca agactctgacaaagcccaagaaatccacagcggcggcagcagcaggaggaggagcgctgcgtct ggcgcccaacgaacccgtatcgacccgcgagcttagaaacaggatttttcccactctgtatgctatatttcaaca gagcaggggccaagaacaagagctgaaaataaaaaacaggtctctgcgatccctcacccgcagctgcctgtatcacaaaagc gaagatcagcttcggcgcacgctggaagacgcggaggctctcttcagtaaatactgcgcgctgactcttaaggactagtttc gcgccctttctcaaatttaagcgcgaaaactacgtcatctccagcggccacacccggcgcca gcacctgtcgtcagcgccattatgagcaaggaaattcccacgccctacatgtggagttaccagccacaaatgggacttgcg gctggagctgcccaagactactcaacccgaataaactacatgagcgcgggaccccacatgatatcccgggtcaacg gaatccgcgcccaccgaaaccgaattctcttggaacaggcggctattaccaccacacctcgta ataaccttaatccccgtagttggcccgctgccctggtgtaccaggaaagtcccgctcccaccactgtggtacttcccagagacgc ccaggccgaagttcagatgactaactcaggggcgcagcttgcgggcggctttcgtcacagggtgcg gtcgcccgggcagggtataactcacctgacaatcagagggcgaggtattcagctcaacgacgagtcgg tgagctcctcgcttggtctccgtccggacgggacatttcagatcggcggcgccggccgtccttcattcacgcctcgtcaggcaatcct aactctgcagacctcgtcctctgagccgcgctctggaggcattggaactctgcaatttat tgaggagtttgtgccatcggtctactttaaccccttctcgggacctcccggccact atccggatcaatttattcctaactttgacgcggtaaaggactcggcggacggctacgactgaatgt taagtggagaggcagagcaactgcgcctgaaacacctggtccactgtcgccgccacaagtgctttgcccgcgac tccggtgagttttgctactttgaattgcccgaggatcatatcgagggcccggcgcacggcgtccggcttaccgcccagggagag cttgcccgtagcctgattcgggagtttacccagcgccccctgctagttgagcgggacaggggaccctgtgttctcac tgtgatttgcaactgtcctaaccttggattacatcaagatcctctagttataactagagtacccgg ggatcttattccctttaactaataaaaaaaaataataaagcatcacttaccttaaaatcagttagcaaatttctgt ccagtttattcagcagacctccttgccctcctcccagctctggtattgcagcttcctcctggc tgcaaactttctccacaatctaaatggaatgtcagtttcctcctgttcctgtccatccgcacccactatcttc atgttgttgcagatgaagcgcgcaagaccgtctgaagataccttcaaccccgtgtatccatatgacacggaaaccgg tcctccaactgtgccttttcttactcctccctttgtatcccccaatgggtttcaagagagtccccct ggggtactctctttgcgcctatccgaacctctagttacctccaatggcatgcttgcgctcaaaatgggcaacggcctctctct ggacgaggccggcaaccttacctcccaaaatgtaaccactgtgagcccacctctcaaaaaaaccaagtcaaaca taaacctggaaatatctgcacccctcacagttacctcagaagccctaactgtggctgccgccgcacctctaatggtcgcgg gcaacacactcaccatgcaatcacaggccccgctaaccgtgcacgactccaaacttagcattgccacccaagga cccctcacagtgtcagaaggaaagctagccctgcaaacatcaggccccctcaccaccaccgatagcagtacccttactat cactgcctcaccccctctaactactgccactggtagcttgggcattgacttgaaagagcccatttatacacaaaatggaaaac taggactaaagtacggggctcctttgcatgtaacagacgacctaaacactttgaccgtagcaact ggtccaggtgtgactattaataatacttccttgcaaactaaagttactggagccttgggttttgattcacaaggcaatatgca acttaatgtagcaggaggactaaggattgattctcaaaacagacgccttatacttgatgttagttatccgtttgatg ctcaaaaccaactaaatctaagactaggacagggccctctttttataaactcagcccacaacttggatattaacta caacaaaggcctttacttgtttacagcttcaaacaattccaaaaagcttgaggttaacctaagcactgc caaggggttgatgtttgacgctacagccatagccattaatgcagga gatgggcttgaatttggttcacctaatgcaccaaacacaaatcccctcaaaacaaaaattgg ccatggcctagaatttgattcaaacaaggctatggttcctaaactaggaactg gccttagttttgacagcacaggtgccattacagtaggaaacaaaaataatgataagctaa ctttgtggaccacaccagctccatctcctaactgtagactaaatgcagagaaag atgctaaactcactttggtcttaacaaaatgtggcagtcaaatacttgctacagtttcagttt tggctgttaaaggcagtttggctccaatatctggaacagttcaaagtgctcatcttattataagatttgacgaaaatggagt gctactaaacaattccttcctggacccagaatattggaactttagaaatggagatcttactgaaggcacagcctatacaaac gctgttggatttatgcctaacctatcagcttatccaaaatctcacggtaaaactgccaaaagtaacatt gtcagtcaagtttacttaaacggagacaaaactaaacctgtaacactaaccattacac taaacggtacacaggaaacaggagacacaactccaagtgcatactctatgtcattttcatg ggactggtctggccacaactacattaatgaaatatttgcca catcctcttacactttttcatacattgcccaagaataaagaatcgtttgtgttatg tttcaacgtgtttatttttcaattgcagaaaatttcaagtcatttttcatt cagtagtatagccccaccaccacatagcttatacagatcaccgtaccttaatcaaactcacagaaccctag tattcaacctgccacctccctcccaacacacagagtacacagtcctttctccccggctggccttaaaaagc atcatatcatgggtaacagacatattcttaggtgttatattccacacggtttcctg tcgagccaaacgctcatcagtgatattaataaactccccgggcagctcacttaagttcatgtcgct gtccagctgctgagccacaggctgctgtccaacttgcggttgcttaacgggcggcgaaggagaagtccacgc ctacatgggggtagagtcataatcgtgcatcaggatagg gcggtggtgctgcagcagcgcgcgaataaactgctgccgccgccgctccgtcctgcaggaatacaacatggcagtggtctcctcag cgatgattcgcaccgcccgcagcataaggcgccttgtcctccgggcacagcagcgcaccctgatctcacttaaatcagcacag taactgcagcacagcaccacaatattgttcaaaatcccacagtgcaaggcgct gtatccaaagctcatggcggggaccacagaacccacgtggccatcataccacaagcgcaggtagattaa gtggcgacccctcataaacacgctggacataaacattacctct tttggcatgttgtaattcaccacctcccggtaccatataaacctctgattaaacatggcgccatccaccaccatcctaaaccagctgg ccaaaacctgcccgccggctatacactgcagggaaccgggactggaacaatgacagtggagagcccaggactcgtaaccatggat catcatgctcgtcatgatatcaatgttggcacaacacaggcacacgtgcatac acttcctcaggattacaagctcctcccgcgttagaaccatatcccagggaacaacccattcctgaatcagc gtaaatcccacactgcagggaagacctcgcacgtaactcacg ttgtgcattgtcaaagtgttacattcgggcagcagcggatgatcctccagtatggtagc gcgggtttctgtctcaaaaggaggtagacgatccctactgtacggagtgcgccga gacaaccgagatcgtgttggtcgtagtgtcatgccaaatggaacgccggacgtagtcatattt cctgaagcaaaaccaggtgcgggcgtgacaaacagatctgcgtctccgg tctcgccgcttagatcgctctgtgtagtagttgtagtatatccactctctcaaagcatccaggcgccccc tggcttcgggttctatgtaaactccttcatgcgccgctgccctgat aacatccaccaccgcagaataagccacacccagccaacctacacattcgttctgcgagtca cacacgggaggagcgggaagagctggaagaaccatgtttttttttttattccaaa agattatccaaaacctcaaaatgaagatctattaagtgaacgcgctcccctccggtggcgtggtcaaactc tacagccaaagaacagataatggcatttgtaagatgttgcaca atggcttccaaaaggcaaacggccctcacgtccaagtggacgtaaaggctaaacccttcagggtgaatctcctctat aaacattccagcaccttcaaccatgcccaaataattc tcatctcgccaccttctcaatatatctctaagcaaatcccgaatattaagtccggccattgtaaaaatc tgctccagagcgccctccaccttcagcctcaagcagcgaatcatga ttgcaaaaattcaggttcctcacagacctgtataagattcaaaagcgg aacattaacaaaaataccgcgatcccgtaggtcccttcgcagggccagctgaacataatcgtgcagg tctgcacggaccagcgcggccacttccccgccaggaaccttgacaaaagaacccacactgattatgaca cgcatactcggagctatgctaaccagcgtagccccgatgtaa gctttgttgcatgggcggcgatataaaatgcaaggtgctgctcaaaaaatcaggcaaagcctcgcgcaaaaaagaa agcacatcgtagtcatgctcatgcagataaaggcag gtaagctccggaaccaccacagaaaaagacaccatttttctctcaaacatgtctgcgggtttctgcataaacacaaaataaa ataacaaaaaaacatttaaacattagaagcctg tcttacaacaggaaaaacaacccttataagcataagacggactacggccatgccg gcgtgaccgtaaaaaaactggtcaccgtgattaaaaagcaccaccgacagctcctc ggtcatgtccggagtcataatgtaagactcggtaaacacatcaggttgattcatcggtcagtgc taaaaagcgaccgaaatagcccgggggaatacatacccgcaggcgtag agacaacattacagcccccataggaggtataacaaaattaataggagagaaaaacacataaacacctg aaaaaccctcctgcctaggcaaaatagcaccctcccgctccag aacaacatacagcgcttcacagcggcagcctaacagtcagccttaccagtaaa aaagaaaacctattaaaaaaacaccactcgacacggcaccagctcaatcagtcacagt gtaaaaaagggccaagtgcagagcgagtatatataggactaaaaaatgacgtaacggttaaagtccacaaaaaacacccagaaaaccgcac gcgaacctacgcccagaa acgaaagccaaaaaacccacaacttcctcaaatcgtcacttccgttttcccacgttacgtaacttcccatttt aagaaaactacaattcccaacacatacaagttactccgc cctaaaacctacgtcacccgccccgttcccacgccccgcgccacgtcacaaactccaccccctcattatcatattggcttcaa tccaaaataaggtatattattgatgatnnn Nucleic acid sequence of the pAdROSd vector (SEQ ID NO: 12). nnttaattaaggatccnnncctgtcctcgaccgatgcccttgagagccttcaacccagtcagctccttccggtgggcgcggggcatgactatc gtcgccgcacttatgactgtcttctttatcatgcaactcgtaggacaggtgccggcagcgctctgggtcattttcggcgaggaccgctttcgctgg agcgcgacgatgatcggcctgtcgcttgcggtattcggaatcttgcacgccctcgctcaagccttcgtcactggtcccgccaccaaacgtttcg gcgagaagcaggccattatcgccggcatggcggccgacgcgctgggctacgtcttgctggcgttcgcgacgcgaggctggatggccttccc cattatgattcttctcgcttccggcggcatcgggatgcccgcgttgcaggccatgctgtccaggcaggtagatgacgaccatcagggacagctt caaggatcgctcgcggctcttaccagcctaacttcgatcactggaccgctgatcgtcacggcgatttatgccgcctcggcgagcacatggaac gggttggcatggattgtaggcgccgccctataccttgtctgcctccccgcgttgcgtcgcggtgcatggagccgggccacctcgacctgaatg gaagccggcggcacctcgctaacggattcaccactccaagaattggagccaatcaattcttgcggagaactgtgaatgcgcaaaccaaccctt ggcagaacatatccatcgcgtccgccatctccagcagccgcacgcggcgcatctcgggcagcgttgggtcctggccacgggtgcgcatgat cgtgctcctgtcgttgaggacccggctaggctggcggggttgccttactggttagcagaatgaatcaccgatacgcgagcgaacgtgaagcg actgctgctgcaaaacgtctgcgacctgagcaacaacatgaatggtcttcggtttccgtgtttcgtaaagtctggaaacgcggaagtcagcgcc ctgcaccattatgttccggatctgcatcgcaggatgctgctggctaccctgtggaacacctacatctgtattaacgaagcgctggcattgaccctg agtgatttttctctggtcccgccgcatccataccgccagttgtttaccctcacaacgttccagtaaccgggcatgttcatcatcagtaacccgtatc gtgagcatcctctctcgtttcatcggtatcattacccccatgaacagaaattcccccttacacggaggcatcaagtgaccaaacaggaaaaaacc gcccttaacatggcccgctttatcagaagccagacattaacgcttctggagaaactcaacgagctggacgcggatgaacaggcagacatctgt gaatcgcttcacgaccacgctgatgagctttaccgcagctgcctcgcgcgtttcggtgatgacggtgaaaacctctgacacatgcagctcccg gagacggtcacagcttgtctgtaagcggatgccgggagcagacaagcccgtcagggcgcgtcagcgggtgttggcgggtgtcggggcgc agccatgacccagtcacgtagcgatagcggagtgtatactggcttaactatgcggcatcagagcagattgtactgagagtgcaccatatgcggt gtgaaataccgcacagatgcgtaaggagaaaataccgcatcaggcgctcttccgcttcctcgctcactgactcgctgcgctcggtcgttcggct gcggcgagcggtatcagctcactcaaaggcggtaatacggttatccacagaatcaggggataacgcaggaaagaacatgtgagcaaaagg ccagcaaaaggccaggaaccgtaaaaaggccgcgttgctggcgtttttccataggctccgcccccctgacgagcatcacaaaaatcgacgct caagtcagaggtggcgaaacccgacaggactataaagataccaggcgtttccccctggaagctccctcgtgcgctctcctgttccgaccctgc cgcttaccggatacctgtccgcctttctcccttcgggaagcgtggcgctttctcaatgctcacgctgtaggtatctcagttcggtgtaggtcgttcg ctccaagctgggctgtgtgcacgaaccccccgttcagcccgaccgctgcgccttatccggtaactatcgtcttgagtccaacccggtaagaca cgacttatcgccactggcagcagccactggtaacaggattagcagagcgaggtatgtaggcggtgctacagagttcttgaagtggtggcctaa ctacggctacactagaaggacagtatttggtatctgcgctctgctgaagccagttaccttcggaaaaagagttggtagctcttgatccggcaaac aaaccaccgctggtagcggtggtttttttgtttgcaagcagcagattacgcgcagaaaaaaaggatctcaagaagatcctttgatcttttctacgg ggtctgacgctcagtggaacgaaaactcacgttaagggattttggtcatgagattatcaaaaaggatcttcacctagatccttttaaattaaaaatg aagttttaaatcaatctaaagtatatatgagtaaacttggtctgacagttaccaatgcttaatcagtgaggcacctatctcagcgatctgtctatttcgt tcatccatagttgcctgactccccgtcgtgtagataactacgatacgggagggcttaccatctggccccagtgctgcaatgataccgcgagacc cacgctcaccggctccagatttatcagcaataaaccagccagccggaagggccgagcgcagaagtggtcctgcaactttatccgcctccatc cagtctattaattgttgccgggaagctagagtaagtagttcgccagttaatagtttgcgcaacgttgttgnnaaaaaggatcttcacctagatccttt tcacgtagaaagccagtccgcagaaacggtgctgaccccggatgaatgtcagctactgggctatctggacaagggaaaacgcaagcgcaaa gagaaagcaggtagcttgcagtgggcttacatggcgatagctagactgggcggttttatggacagcaagcgaaccggaattgccagctgggg cgccctctggtaaggttgggaagccctgcaaagtaaactggatggctttctcgccgccaaggatctgatggcgcaggggatcaagctctgatc aagagacaggatgaggatcgtttcgcatgattgaacaagatggattgcacgcaggttctccggccgcttgggtggagaggctattcggctatg actgggcacaacagacaatcggctgctctgatgccgccgtgttccggctgtcagcgcaggggcgcccggttctttttgtcaagaccgacctgt ccggtgccctgaatgaactgcaagacgaggcagcgcggctatcgtggctggccacgacgggcgttccttgcgcagctgtgctcgacgttgtc actgaagcgggaagggactggctgctattgggcgaagtgccggggcaggatctcctgtcatctcaccttgctcctgccgagaaagtatccatc atggctgatgcaatgcggcggctgcatacgcttgatccggctacctgcccattcgaccaccaagcgaaacatcgcatcgagcgagcacgtac tcggatggaagccggtcttgtcgatcaggatgatctggacgaagagcatcaggggctcgcgccagccgaactgttcgccaggctcaaggcg agcatgcccgacggcgaggatctcgtcgtgacccatggcgatgcctgcttgccgaatatcatggtggaaaatggccgcttttctggattcatcg actgtggccggctgggtgtggcggaccgctatcaggacatagcgttggctacccgtgatattgctgaagagcttggcggcgaatgggctgac cgcttcctcgtgctttacggtatcgccgctcccgattcgcagcgcatcgccttctatcgccttcttgacgagttcttctgaattttgttaaaatttttg ttaaatcagctcattttttaaccaataggccgaaatcggcaacatcccttataaatcaaaagaatagaccgcgatagggttgagtgttgttccagtttg gaacaagagtccactattaaagaacgtggactccaacgtcaaagggcgaaaaaccgtctatcagggcgatggcccactacgtgaaccatcac ccaaatcaagttttttgcggtcgaggtgccgtaaagctctaaatcggaaccctaaagggagcccccgatttagagcttgacggggaaagccgg cgaacgtggcgagaaaggaagggaagaaagcgaaaggagcgggcgctagggcgctggcaagtgtagcggtcacgctgcgcgtaacca ccacacccgcgcgcttaatgcgccgnnnnnnttaattaannntcccttccagctctctgccccttttggattgaagccaatatgataatgaggg ggtggagtttgtgacgtggcgcggggcgtgggaacggggcgggtgacgtagtagtgtggcggaagtgtgatgttgcaagtgtggcggaac acatgtaagcgacggatgtggcaaaagtgacgtttttggtgtgcgccggtgtacacaggaagtgacaattttcgcgcggttttaggcggatgttg tagtaaatttgggcgtaaccgagtaagatttggccattttcgcgggaaaactgaataagaggaagtgaaatctgaataattttgtgttactcatagc gcgtaannngtagttattaatagtaatcaattacggggtcattagttcatagcccatatatggagttccgcgttacataacttacggtaaatggccc gcctggctgaccgcccaacgacccccgcccattgacgtcaataatgacgtatgttcccatagtaacgccaatagggactttccattgacgtcaat gggtggagtatttacggtaaactgcccacttggcagtacatcaagtgtatcatatgccaagtacgccccctattgacgtcaatgacggtaaatgg cccgcctggcattatgcccagtacatgaccttatgggactttcctacttggcagtacatctacgtattagtcatcgctattaccatggtgatgcggttt tggcagtacatcaatgggcgtggatagcggtttgactcacggggatttccaagtctccaccccattgacgtcaatgggagtttgttttggcacca aaatcaacgggactttccaaaatgtcgtaacaactccgccccattgacgcaaatgggcggtaggcgtgtacggtgggaggtctatataagcag agctggtttagtgaaccgtcagatccgctagaccatggcctcctccgaggacgtcatcaaggagttcatgcgcttcaaggtgcgcatggaggg ctccgtgaacggccacgagttcgagatcgagggcgagggcgagggccgcccctacgagggcacccagaccgccaagctgaaggtgacc aagggcggccccctgcccttcgcctgggacatcctgtcccctcagttccagtacggctccaaggcctacgtgaagcaccccgccgacatccc cgactacttgaagctgtccttccccgagggcttcaagtgggagcgcgtgatgaacttcgaggacggcggcgtggtgaccgtgacccaggact cctccctgcaggacggcgagttcatctacaaggtgaagctgcgcggcaccaacttcccctccgacggccccgtaatgcagaagaagaccat gggctgggaggcctccaccgagcggatgtaccccgaggacggcgccctgaagggcgagatcaagatgaggctgaagctgaaggacggc ggccactacgacgccgaggtcaagaccacctacatggccaagaagcccgtgcagctgcccggcgcctacaagaccgacatcaagctgga catcacctcccacaacgaggactacaccatcgtggaacagtacgagcgcgccgagggccgccactccaccggcgccaatccaccggatct agataactgatcataatcagccataccacatttgtagaggttttacttgctttaaaaaacctcccacacctccccctgaacctgaaacataaaatga atgcaattgttgttgttaacttgtttattgcagcttataatggttacaaataaagcaatagcatcacaaatttcacaaataaagcatttttttcactgc attctagttgtggtttgtccaaactcatcaatgtatcttaacgcgtctctagttattaatagtaatcaattacggggtcattagttcatagcccatat atggagttccgcgttacataacttacggtaaatggcccgcctggctgaccgcccaacgacccccgcccattgacgtcaataatgacgtatgttcccata gtaacgccaatagggactttccattgacgtcaatgggtggagtatttacggtaaactgcccacttggcagtacatcaagtgtatcatatgccaagt acgccccctattgacgtcaatgacggtaaatggcccgcctggcattatgcccagtacatgaccttatgggactttcctacttggcagtacatctac gtattagtcatcgctattaccatggtgatgcggttttggcagtacatcaatgggcgtggatagcggtttgactcacggggatttccaagtctccacc ccattgacgtcaatgggagtttgttttggaaccaaaatcaacgggactttccaaaatgtcgtaacaactccgccccattgacgcaaatgggcggt aggcgtgtacggtgggaggtctatataagcagagctctccctatcagtgatagagatctccctatcagtgatagagatctccctatcagtgatag agatctccctatcagtgatagagatcgagctgtttagtgaaccgtcagatcgcctggagacgccatccacgctgttttgacctccatagaagaca ccgaattcaggggatccaatcggaaagcggacgcggaatttaaattgatttttgcggtataagaatatatactgatatgtatacccgaagtatgtc aaaaagaggtatgctatgaagcagcgtattacagtgacagttgacagcgacagctatcagttgctcaaggcatatatgatgtcaatatctccggt ctggtaagcacaaccatgcagaatgaagcccgtcgtctgcgtgccgaacgctggaaagcggaaaatcaggaagggatggctgaggtcgcc cggtttattgaaatgaacggctcttttgctgacgagaacaggggctggtgaaatgcagtttaaggtttacacctataaaagagagagccgttatc gtctgtttgtggatgtacagagtgatattattgacacgcccgggcgacggatggtgatccccctggccagtgcacgtctgctgtcagataaagtc tcccgtgaactttacccggtggtgcatatcggggatgaaagctggcgcatgatgaccaccgatatggccagtgtgccggtctccgttatcggg gaagaagtggctgatctcagccaccgcgaaaatgacatcaaaaacgccattaacctgatgttctggggaatataaatgtcaggctcccttatac acagccagtctgcagctcgctcttcatttaaatcgagtatcccgtgagcgctttctagagatatcggccgctaaacccgctgatcagcctcgact gtgccttctagttgccagccatctgttgtttgcccctcccccgtgccttccttgaccctggaaggtgccactcccactgtcctttcctaataaaatga ggaaattgcatcgcattgtctgagtaggtgtcattctattctggggggtggggtggggcaggacagcaagggggaggattgggaagacaata gcaggcatgctggggatgcggtgggctctatggcttctgaggcggaaagaaccaggatctgctaggatctnntaagggtgggaaagaatata taaggtgggggtcttatgtagttttgtatctgttttgcagcagccgccgccgccatgagcaccaactcgtttgatggaagcattgtgagctcatattt gacaacgcgcatgcccccatgggccggggtgcgtcagaatgtgatgggctccagcattgatggtcgccccgtcctgcccgcaaactctacta ccttgacctacgagaccgtgtctggaacgccgttggagactgcagcctccgccgccgcttcagccgctgcagccaccgcccgcgggattgtg actgactttgctttcctgagcccgcttgcaagcagtgcagcttcccgttcatccgcccgcgatgacaagttgacggctcttttggcacaattggatt ctttgacccgggaacttaatgtcgtttctcagcagctgttggatctgcgccagcaggtttctgccctgaaggcttcctcccctcccaatgcggttta aaacataaataaaaaaccagactctgtttggatttggatcaagcaagtgtcttgctgtctttatttaggggttttgcgcgcgcggtaggcccggga ccagcggtctcggtcgttgagggtcctgtgtattttttccaggacgtggtaaaggtgactctggatgttcagatacatgggcataagcccgtctct ggggtggaggtagcaccactgcagagcttcatgctgcggggtggtgttgtagatgatccagtcgtagcaggagcgctgggcgtggtgcctaa aaatgtctttcagtagcaagctgattgccaggggcaggcccttggtgtaagtgtttacaaagcggttaagctgggatgggtgcatacgtgggga tatgagatgcatcttggactgtatttttaggttggctatgttcccagccatatccctccggggattcatgttgtgcagaaccaccagcacagtgtatc cggtgcacttgggaaatttgtcatgtagcttagaaggaaatgcgtggaagaacttggagacgcccttgtgacctccaagattttccatgcattcgt ccataatgatggcaatgggcccacgggcggcggcctgggcgaagatatttctgggatcactaacgtcatagttgtgttccaggatgagatcgtc ataggccatttttacaaagcgcgggcggagggtgccagactgcggtataatggttccatccggcccaggggcgtagttaccctcacagatttg catttcccacgctttgagttcagatggggggatcatgtctacctgcggggcgatgaagaaaacggtttccggggtaggggagatcagctggga agaaagcaggttcctgagcagctgcgacttaccgcagccggtgggcccgtaaatcacacctattaccgggtgcaactggtagttaagagagc tgcagctgccgtcatccctgagcaggggggccacttcgttaagcatgtccctgactcgcatgttttccctgaccaaatccgccagaaggcgctc gccgcccagcgatagcagttcttgcaaggaagcaaagtttttcaacggtttgagaccgtccgccgtaggcatgcttttgagcgtttgaccaagc agttccaggcggtcccacagctcggtcacctgctctacggcatctcgatccagcatatctcctcgtttcgcgggttggggcggctttcgctgtac ggcagtagtcggtgctcgtccagacgggccagggtcatgtctttccacgggcgcagggtcctcgtcagcgtagtctgggtcacggtgaaggg gtgcgctccgggctgcgcgctggccagggtgcgcttgaggctggtcctgctggtgctgaagcgctgccggtcttcgccctgcgcgtcggcca ggtagcatttgaccatggtgtcatagtccagcccctccgcggcgtggcccttggcgcgcagcttgcccttggaggaggcgccgcacgaggg gcagtgcagacttttgagggcgtagagcttgggcgcgagaaataccgattccggggagtaggcatccgcgccgcaggccccgcagacggt ctcgcattccacgagccaggtgagctctggccgttcggggtcaaaaaccaggtttcccccatgctttttgatgcgtttcttacctctggtttccatga gccggtgtccacgctcggtgacgaaaaggctgtccgtgtccccgtatacagacttgagaggcctgtcctcgagcggtgttccgcggtcctcct cgtatagaaactcggaccactctgagacaaaggctcgcgtccaggccagcacgaaggaggctaagtgggaggggtagcggtcgttgtcca ctagggggtccactcgctccagggtgtgaagacacatgtcgccctcttcggcatcaaggaaggtgattggtttgtaggtgtaggccacgtgac cgggtgttcctgaaggggggctataaaagggggtgggggcgcgttcgtcctcactctcttccgcatcgctgtctgcgagggccagctgttggg gtgagtactccctctgaaaagcgggcatgacttctgcgctaagattgtcagtttccaaaaacgaggaggatttgatattcacctggcccgcggtg atgcctttgagggtggccgcatccatctggtcagaaaagacaatctttttgttgtcaagcttggtggcaaacgacccgtagagggcgttggaca gcaacttggcgatggagcgcagggtttggtttttgtcgcgatcggcgcgctccttggccgcgatgtttagctgcacgtattcgcgcgcaacgca ccgccattcgggaaagacggtggtgcgctcgtcgggcaccaggtgcacgcgccaaccgcggttgtgcagggtgacaaggtcaacgctggt ggctacctctccgcgtaggcgctcgttggtccagcagaggcggccgcccttgcgcgagcagaatggcggtagggggtctagctgcgtctcg tccggggggtctgcgtccacggtaaagaccccgggcagcaggcgcgcgtcgaagtagtctatcttgcatccttgcaagtctagcgcctgctg ccatgcgcgggcggcaagcgcgcgctcgtatgggttgagtgggggaccccatggcatggggtgggtgagcgcggaggcgtacatgccgc aaatgtcgtaaacgtagaggggctctctgagtattccaagatatgtagggtagcatcttccaccgcggatgctggcgcgcacgtaatcgtatagt tcgtgcgagggagcgaggaggtcgggaccgaggttgctacgggcgggctgctctgctcggaagactatctgcctgaagatggcatgtgagt tggatgatatggttggacgctggaagacgttgaagctggcgtctgtgagacctaccgcgtcacgcacgaaggaggcgtaggagtcgcgcag cttgttgaccagctcggcggtgacctgcacgtctagggcgcagtagtccagggtttccttgatgatgtcatacttatcctgtcccttttttttcca cagctcgcggttgaggacaaactcttcgcggtctttccagtactcttggatcggaaacccgtcggcctccgaacggtaagagcctagcatgtagaac tggttgacggcctggtaggcgcagcatcccttttctacgggtagcgcgtatgcctgcgcggccttccggagcgaggtgtgggtgagcgcaaa ggtgtccctgaccatgactttgaggtactggtatttgaagtcagtgtcgtcgcatccgccctgctcccagagcaaaaagtccgtgcgctttttgga acgcggatttggcagggcgaaggtgacatcgttgaagagtatctttcccgcgcgaggcataaagttgcgtgtgatgcggaagggtcccggca cctcggaacggttgttaattacctgggcggcgagcacgatctcgtcaaagccgttgatgttgtggcccacaatgtaaagttccaagaagcgcg ggatgcccttgatggaaggcaattttttaagttcctcgtaggtgagctcttcaggggagctgagcccgtgctctgaaagggcccagtctgcaag atgagggttggaagcgacgaatgagctccacaggtcacgggccattagcatttgcaggtggtcgcgaaaggtcctaaactggcgacctatgg ccattttttctggggtgatgcagtagaaggtaagcgggtcttgttcccagcggtcccatccaaggttcgcggctaggtctcgcgcggcagtcact agaggctcatctccgccgaacttcatgaccagcatgaagggcacgagctgcttcccaaaggcccccatccaagtataggtctctacatcgtag gtgacaaagagacgctcggtgcgaggatgcgagccgatcgggaagaactggatctcccgccaccaattggaggagtggctattgatgtggt gaaagtagaagtccctgcgacgggccgaacactcgtgctggcttttgtaaaaacgtgcgcagtactggcagcggtgcacgggctgtacatcct gcacgaggttgacctgacgaccgcgcacaaggaagcagagtgggaatttgagcccctcgcctggcgggtttggctggtggtcttctacttcg gctgcttgtccttgaccgtctggctgctcgaggggagttacggtggatcggaccaccacgccgcgcgagcccaaagtccagatgtccgcgcg cggcggtcggagcttgatgacaacatcgcgcagatgggagctgtccatggtctggagctcccgcggcgtcaggtcaggcgggagctcctgc aggtttacctcgcatagacgggtcagggcgcgggctagatccaggtgatacctaatttccaggggctggttggtggcggcgtcgatggcttgc aagaggccgcatccccgcggcgcgactacggtaccgcgcggcgggcggtgggccgcgggggtgtccttggatgatgcatctaaaagcgg tgacgcgggcgagcccccggaggtagggggggctccggacccgccgggagagggggcaggggcacgtcggcgccgcgcgcgggca ggagctggtgctgcgcgcgtaggttgctggcgaacgcgacgacgcggcggttgatctcctgaatctggcgcctctgcgtgaagacgacggg cccggtgagcttgagcctgaaagagagttcgacagaatcaatttcggtgtcgttgacggcggcctggcgcaaaatctcctgcacgtctcctga gttgtcttgataggcgatctcggccatgaactgctcgatctcttcctcctggagatctccgcgtccggctcgctccacggtggcggcgaggtcgt tggaaatgcgggccatgagctgcgagaaggcgttgaggcctccctcgttccagacgcggctgtagaccacgcccccttcggcatcgcgggc gcgcatgaccacctgcgcgagattgagctccacgtgccgggcgaagacggcgtagtttcgcaggcgctgaaagaggtagttgagggtggtg gcggtgtgttctgccacgaagaagtacataacccagcgtcgcaacgtggattcgttgatatcccccaaggcctcaaggcgctccatggcctcg tagaagtccacggcgaagttgaaaaactgggagttgcgcgccgacacggttaactcctcctccagaagacggatgagctcggcgacagtgtc gcgcacctcgcgctcaaaggctacaggggcctcttcttcttcttcaatctcctcttccataagggcctccccttcttcttcttctggcggcggtggg ggaggggggacacggcggcgacgacggcgcaccgggaggcggtcgacaaagcgctcgatcatctccccgcggcgacggcgcatggtc tcggtgacggcgcggccgttctcgcgggggcgcagttggaagacgccgcccgtcatgtcccggttatgggttggcggggggctgccatgc ggcagggatacggcgctaacgatgcatctcaacaattgttgtgtaggtactccgccgccgagggacctgagcgagtccgcatcgaccggatc ggaaaacctctcgagaaaggcgtctaaccagtcacagtcgcaaggtaggctgagcaccgtggcgggcggcagcgggcggcggtcggggt tgtttctggcggaggtgctgctgatgatgtaattaaagtaggcggtcttgagacggcggatggtcgacagaagcaccatgtccttgggtccggc ctgctgaatgcgcaggcggtcggccatgccccaggcttcgttttgacatcggcgcaggtctttgtagtagtcttgcatgagcctttctaccggca cttcttcttctccttcctcttgtcctgcatctcttgcatctatcgctgcggcggcggcggagtttggccgtaggtggcgccctcttcctcccatgcgt gtgaccccgaagcccctcatcggctgaagcagggctaggtcggcgacaacgcgctcggctaatatggcctgctgcacctgcgtgagggtag actggaagtcatccatgtccacaaagcggtggtatgcgcccgtgttgatggtgtaagtgcagttggccataacggaccagttaacggtctggtg acccggctgcgagagctcggtgtacctgagacgcgagtaagccctcgagtcaaatacgtagtcgttgcaagtccgcaccaggtactggtatc ccaccaaaaagtgcggcggcggctggcggtagaggggccagcgtagggtggccggggctccgggggcgagatcttccaacataaggcg atgatatccgtagatgtacctggacatccaggtgatgccggcggcggtggtggaggcgcgcggaaagtcgcggacgcggttccagatgttg cgcagcggcaaaaagtgctccatggtcgggacgctctggccggtcaggcgcgcgcaatcgttgacgctctaccgtgcaaaaggagagcct gtaagcgggcactcttccgtggtctggtggataaattcgcaagggtatcatggcggacgaccggggttcgagccccgtatccggccgtccgc cgtgatccatgcggttaccgcccgcgtgtcgaacccaggtgtgcgacgtcagacaacgggggagtgctccttttggcttccttccaggcgcgg cggctgctgcgctagcttttttggccactggccgcgcgcagcgtaagcggttaggctggaaagcgaaagcattaagtggctcgctccctgtag ccggagggttattttccaagggttgagtcgcgggacccccggttcgagtctcggaccggccggactgcggcgaacgggggtttgcctcccc gtcatgcaagaccccgcttgcaaattcctccggaaacagggacgagccccttttttgcttttcccagatgcatccggtgctgcggcagatgcgc ccccctcctcagcagcggcaagagcaagagcagcggcagacatgcagggcaccctcccctcctcctaccgcgtcaggaggggcgacatc cgcggttgacgcggcagcagatggtgattacgaacccccgcggcgccgggcccggcactacctggacttggaggagggcgagggcctg gcgcggctaggagcgccctctcctgagcggtacccaagggtgcagctgaagcgtgatacgcgtgaggcgtacgtgccgcggcagaacctg tttcgcgaccgcgagggagaggagcccgaggagatgcgggatcgaaagttccacgcagggcgcgagctgcggcatggcctgaatcgcga gcggttgctgcgcgaggaggactttgagcccgacgcgcgaaccgggattagtcccgcgcgcgcacacgtggcggccgccgacctggtaa ccgcatacgagcagacggtgaaccaggagattaactttcaaaaaagctttaacaaccacgtgcgtacgcttgtggcgcgcgaggaggtggct ataggactgatgcatctgtgggactttgtaagcgcgctggagcaaaacccaaatagcaagccgctcatggcgcagctgttccttatagtgcagc acagcagggacaacgaggcattcagggatgcgctgctaaacatagtagagcccgagggccgctggctgctcgatttgataaacatcctgcag agcatagtggtgcaggagcgcagcttgagcctggctgacaaggtggccgccatcaactattccatgcttagcctgggcaagttttacgcccgc aagatataccataccccttacgttcccatagacaaggaggtaaagatcgaggggttctacatgcgcatggcgctgaaggtgcttaccttgagcg acgacctgggcgtttatcgcaacgagcgcatccacaaggccgtgagcgtgagccggcggcgcgagctcagcgaccgcgagctgatgcac agcctgcaaagggccctggctggcacgggcagcggcgatagagaggccgagtcctactttgacgcgggcgctgacctgcgctgggcccc aagccgacgcgccctggaggcagctggggccggacctgggctggcggtggcacccgcgcgcgctggcaacgtcggcggcgtggagga atatgacgaggacgatgagtacgagccagaggacggcgagtactaagcggtgatgtttctgatcagatgatgcaagacgcaacggacccgg cggtgcgggcggcgctgcagagccagccgtccggccttaactccacggacgactggcgccaggtcatggaccgcatcatgtcgctgactg cgcgcaatcctgacgcgttccggcagcagccgcaggccaaccggctctccgcaattctggaagcggtggtcccggcgcgcgcaaacccca cgcacgagaaggtgctggcgatcgtaaacgcgctggccgaaaacagggccatccggcccgacgaggccggcctggtctacgacgcgctg cttcagcgcgtggctcgttacaacagcggcaacgtgcagaccaacctggaccggctggtgggggatgtgcgcgaggccgtggcgcagcgt gagcgcgcgcagcagcagggcaacctgggctccatggttgcactaaacgccttcctgagtacacagcccgccaacgtgccgcggggacag gaggactacaccaactttgtgagcgcactgcggctaatggtgactgagacaccgcaaagtgaggtgtaccagtctgggccagactattttttcc agaccagtagacaaggcctgcagaccgtaaacctgagccaggctttcaaaaacttgcaggggctgtggggggtgcgggctcccacaggcg accgcgcgaccgtgtctagcttgctgacgcccaactcgcgcctgttgctgctgctaatagcgcccttcacggacagtggcagcgtgtcccggg acacatacctaggtcacttgctgacactgtaccgcgaggccataggtcaggcgcatgtggacgagcatactttccaggagattacaagtgtca gccgcgcgctggggcaggaggacacgggcagcctggaggcaaccctaaactacctgctgaccaaccggcggcagaagatcccctcgttg cacagtttaaacagcgaggaggagcgcattttgcgctacgtgcagcagagcgtgagccttaacctgatgcgcgacggggtaacgcccagcg tggcgctggacatgaccgcgcgcaacatggaaccgggcatgtatgcctcaaaccggccgtttatcaaccgcctaatggactacttgcatcgcg cggccgccgtgaaccccgagtatttcaccaatgccatcttgaacccgcactggctaccgccccctggtttctacaccgggggattcgaggtgc ccgagggtaacgatggattcctctgggacgacatagacgacagcgtgttttccccgcaaccgcagaccctgctagagttgcaacagcgcgag caggcagaggcggcgctgcgaaaggaaagcttccgcaggccaagcagcttgtccgatctaggcgctgcggccccgcggtcagatgctagt agcccatttccaagcttgatagggtctcttaccagcactcgcaccacccgcccgcgcctgctgggcgaggaggagtacctaaacaactcgctg ctgcagccgcagcgcgaaaaaaacctgcctccggcatttcccaacaacgggatagagagcctagtggacaagatgagtagatggaagacgt acgcgcaggagcacagggacgtgccaggcccgcgcccgcccacccgtcgtcaaaggcacgaccgtcagcggggtctggtgtgggagga cgatgactcggcagacgacagcagcgtcctggatttgggagggagtggcaacccgtttgcgcaccttcgccccaggctggggagaatgtttt aaaaaaaaaaaagcatgatgcaaaataaaaaactcaccaaggccatggcaccgagcgttggttttcttgtattccccttagtatgcggcgcgcg gcgatgtatgaggaaggtcctcctccctcctacgagagtgtggtgagcgcggcgccagtggcggcggcgctgggttctcccttcgatgctcc cctggacccgccgtttgtgcctccgcggtacctgcggcctaccggggggagaaacagcatccgttactctgagttggcacccctattcgacac cacccgtgtgtacctggtggacaacaagtcaacggatgtggcatccctgaactaccagaacgaccacagcaactttctgaccacggtcattca aaacaatgactacagcccgggggaggcaagcacacagaccatcaatcttgacgaccggtcgcactggggcggcgacctgaaaaccatcct gcataccaacatgccaaatgtgaacgagttcatgtttaccaataagtttaaggcgcgggtgatggtgtcgcgcttgcctactaaggacaatcagg tggagctgaaatacgagtgggtggagttcacgctgcccgagggcaactactccgagaccatgaccatagaccttatgaacaacgcgatcgtg gagcactacttgaaagtgggcagacagaacggggttctggaaagcgacatcggggtaaagtttgacacccgcaacttcagactggggtttga ccccgtcactggtcttgtcatgcctggggtatatacaaacgaagccttccatccagacatcattttgctgccaggatgcggggtggacttcaccc acagccgcctgagcaacttgttgggcatccgcaagcggcaacccttccaggagggctttaggatcacctacgatgatctggagggtggtaac attcccgcactgttggatgtggacgcctaccaggcgagcttgaaagatgacaccgaacagggcgggggtggcgcaggcggcagcaacag cagtggcagcggcgcggaagagaactccaacgcggcagccgcggcaatgcagccggtggaggacatgaacgatcatgccattcgcggc gacacctttgccacacgggctgaggagaagcgcgctgaggccgaagcagcggccgaagctgccgcccccgctgcgcaacccgaggtcg agaagcctcagaagaaaccggtgatcaaacccctgacagaggacagcaagaaacgcagttacaacctaataagcaatgacagcaccttcac ccagtaccgcagctggtaccttgcatacaactacggcgaccctcagaccggaatccgctcatggaccctgctttgcactcctgacgtaacctgc ggctcggagcaggtctactggtcgttgccagacatgatgcaagaccccgtgaccttccgctccacgcgccagatcagcaactttccggtggtg ggcgccgagctgttgcccgtgcactccaagagcttctacaacgaccaggccgtctactcccaactcatccgccagtttacctctctgacccacg tgttcaatcgctttcccgagaaccagattttggcgcgcccgccagcccccaccatcaccaccgtcagtgaaaacgttcctgctctcacagatca cgggacgctaccgctgcgcaacagcatcggaggagtccagcgagtgaccattactgacgccagacgccgcacctgcccctacgtttacaag gccctgggcatagtctcgccgcgcgtcctatcgagccgcactttttgagcaagcatgtccatccttatatcgcccagcaataacacaggctggg gcctgcgcttcccaagcaagatgtttggcggggccaagaagcgctccgaccaacacccagtgcgcgtgcgcgggcactaccgcgcgccct ggggcgcgcacaaacgcggccgcactgggcgcaccaccgtcgatgacgccatcgacgcggtggtggaggaggcgcgcaactacacgc ccacgccgccaccagtgtccacagtggacgcggccattcagaccgtggtgcgcggagcccggcgctatgctaaaatgaagagacggcgg aggcgcgtagcacgtcgccaccgccgccgacccggcactgccgcccaacgcgcggcggcggccctgcttaaccgcgcacgtcgcaccg gccgacgggcggccatgcgggccgctcgaaggctggccgcgggtattgtcactgtgccccccaggtccaggcgacgagcggccgccgc agcagccgcggccattagtgctatgactcagggtcgcaggggcaacgtgtattgggtgcgcgactcggttagcggcctgcgcgtgcccgtg cgcacccgccccccgcgcaactagattgcaagaaaaaactacttagactcgtactgttgtatgtatccagcggcggcggcgcgcaacgaagc tatgtccaagcgcaaaatcaaagaagagatgctccaggtcatcgcgccggagatctatggccccccgaagaaggaagagcaggattacaag ccccgaaagctaaagcgggtcaaaaagaaaaagaaagatgatgatgatgaacttgacgacgaggtggaactgctgcacgctaccgcgccc aggcgacgggtacagtggaaaggtcgacgcgtaaaacgtgttttgcgacccggcaccaccgtagtctttacgcccggtgagcgctccaccc gcacctacaagcgcgtgtatgatgaggtgtacggcgacgaggacctgcttgagcaggccaacgagcgcctcggggagtttgcctacggaaa gcggcataaggacatgctggcgttgccgctggacgagggcaacccaacacctagcctaaagcccgtaacactgcagcaggtgctgcccgc gcttgcaccgtccgaagaaaagcgcggcctaaagcgcgagtctggtgacttggcacccaccgtgcagctgatggtacccaagcgccagcg actggaagatgtcttggaaaaaatgaccgtggaacctgggctggagcccgaggtccgcgtgcggccaatcaagcaggtggcgccgggact gggcgtgcagaccgtggacgttcagatacccactaccagtagcaccagtattgccaccgccacagagggcatggagacacaaacgtcccc ggttgcctcagcggtggcggatgccgcggtgcaggcggtcgctgcggccgcgtccaagacctctacggaggtgcaaacggacccgtggat gtttcgcgtttcagccccccggcgcccgcgcggttcgaggaagtacggcgccgccagcgcgctactgcccgaatatgccctacatccttccat tgcgcctacccccggctatcgtggctacacctaccgccccagaagacgagcaactacccgacgccgaaccaccactggaacccgccgccg ccgtcgccgtcgccagcccgtgctggccccgatttccgtgcgcagggtggctcgcgaaggaggcaggaccctggtgctgccaacagcgcg ctaccaccccagcatcgtttaaaagccggtctttgtggttcttgcagatatggccctcacctgccgcctccgtttcccggtgccgggattccgag gaagaatgcaccgtaggaggggcatggccggccacggcctgacgggcggcatgcgtcgtgcgcaccaccggcggcggcgcgcgtcgc accgtcgcatgcgcggcggtatcctgcccctccttattccactgatcgccgcggcgattggcgccgtgcccggaattgcatccgtggccttgca ggcgcagagacactgattaaaaacaagttgcatgtggaaaaatcaaaataaaaagtctggactctcacgctcgcttggtcctgtaactattttgta gaatggaagacatcaactttgcgtctctggccccgcgacacggctcgcgcccgttcatgggaaactggcaagatatcggcaccagcaatatg agcggtggcgccttcagctggggctcgctgtggagcggcattaaaaatttcggttccaccgttaagaactatggcagcaaggcctggaacag cagcacaggccagatgctgagggataagttgaaagagcaaaatttccaacaaaaggtggtagatggcctggcctctggcattagcggggtgg tggacctggccaaccaggcagtgcaaaataagattaacagtaagcttgatccccgccctcccgtagaggagcctccaccggccgtggagac agtgtctccagaggggcgtggcgaaaagcgtccgcgccccgacagggaagaaactctggtgacgcaaatagacgagcctccctcgtacga ggaggcactaaagcaaggcctgcccaccacccgtcccatcgcgcccatggctaccggagtgctgggccagcacacacccgtaacgctgga cctgcctccccccgccgacacccagcagaaacctgtgctgccaggcccgaccgccgttgttgtaacccgtcctagccgcgcgtccctgcgcc gcgccgccagcggtccgcgatcgttgcggcccgtagccagtggcaactggcaaagcacactgaacagcatcgtgggtctgggggtgcaat ccctgaagcgccgacgatgcttctgaatagctaacgtgtcgtatgtgtgtcatgtatgcgtccatgtcgccgccagaggagctgctgagccgcc gcgcgcccgctttccaagatggctaccccttcgatgatgccgcagtggtcttacatgcacatctcgggccaggacgcctcggagtacctgagc cccgggctggtgcagtttgcccgcgccaccgagacgtacttcagcctgaataacaagtttagaaaccccacggtggcgcctacgcacgacgt gaccacagaccggtcccagcgtttgacgctgcggttcatccctgtggaccgtgaggatactgcgtactcgtacaaggcgcggttcaccctagc tgtgggtgataaccgtgtgctggacatggcttccacgtactttgacatccgcggcgtgctggacaggggccctacttttaagccctactctggca ctgcctacaacgccctggctcccaagggtgccccaaatccttgcgaatgggatgaagctgctactgctcttgaaataaacctagaagaagagg acgatgacaacgaagacgaagtagacgagcaagctgagcagcaaaaaactcacgtatttgggcaggcgccttattctggtataaatattacaa aggagggtattcaaataggtgtcgaaggtcaaacacctaaatatgccgataaaacatttcaacctgaacctcaaataggagaatctcagtggta cgaaactgaaattaatcatgcagctgggagagtccttaaaaagactaccccaatgaaaccatgttacggttcatatgcaaaacccacaaatgaa aatggagggcaaggcattcttgtaaagcaacaaaatggaaagctagaaagtcaagtggaaatgcaatttttctcaactactgaggcgaccgca ggcaatggtgataacttgactcctaaagtggtattgtacagtgaagatgtagatatagaaaccccagacactcatatttcttacatgcccactatta aggaaggtaactcacgagaactaatgggccaacaatctatgcccaacaggcctaattacattgcttttagggacaattttattggtctaatgtatta caacagcacgggtaatatgggtgttctggcgggccaagcatcgcagttgaatgctgttgtagatttgcaagacagaaacacagagctttcatac cagcttttgcttgattccattggtgatagaaccaggtacttttctatgtggaatcaggctgttgacagctatgatccagatgttagaattattgaaaa tcatggaactgaagatgaacttccaaattactgctttccactgggaggtgtgattaatacagagactcttaccaaggtaaaacctaaaacaggtcag gaaaatggatgggaaaaagatgctacagaattttcagataaaaatgaaataagagttggaaataattttgccatggaaatcaatctaaatgccaa cctgtggagaaatttcctgtactccaacatagcgctgtatttgcccgacaagctaaagtacagtccttccaacgtaaaaatttctgataacccaaac acctacgactacatgaacaagcgagtggtggctcccgggttagtggactgctacattaaccttggagcacgctggtcccttgactatatggaca acgtcaacccatttaaccaccaccgcaatgctggcctgcgctaccgctcaatgttgctgggcaatggtcgctatgtgcccttccacatccaggtg cctcagaagttctttgccattaaaaacctccttctcctgccgggctcatacacctacgagtggaacttcaggaaggatgttaacatggttctgcag agctccctaggaaatgacctaagggttgacggagccagcattaagtttgatagcatttgcctttacgccaccttcttccccatggcccacaacac cgcctccacgcttgaggccatgcttagaaacgacaccaacgaccagtcctttaacgactatctctccgccgccaacatgctctaccctataccc gccaacgctaccaacgtgcccatatccatcccctcccgcaactgggcggctttccgcggctgggccttcacgcgccttaagactaaggaaac cccatcactgggctcgggctacgacccttattacacctactctggctctataccctacctagatggaaccttttacctcaaccacacctttaagaag gtggccattacctttgactcttctgtcagctggcctggcaatgaccgcctgcttacccccaacgagtttgaaattaagcgctcagttgacgggga gggttacaacgttgcccagtgtaacatgaccaaagactggttcctggtacaaatgctagctaactacaacattggctaccagggcttctatatccc agagagctacaaggaccgcatgtactccttctttagaaacttccagcccatgagccgtcaggtggtggatgatactaaatacaaggactaccaa caggtgggcatcctacaccaacacaacaactctggatttgttggctaccttgcccccaccatgcgcgaaggacaggcctaccctgctaacttcc cctatccgcttataggcaagaccgcagttgacagcattacccagaaaaagtttctttgcgatcgcaccctttggcgcatcccattctccagtaactt tatgtccatgggcgcactcacagacctgggccaaaaccttctctacgccaactccgcccacgcgctagacatgacttttgaggtggatcccatg gacgagcccacccttctttatgttttgtttgaagtctttgacgtggtccgtgtgcaccggccgcaccgcggcgtcatcgaaaccgtgtacctgcgc acgcccttctcggccggcaacgccacaacataaagaagcaagcaacatcaacaacagctgccgccatgggctccagtgagcaggaactga aagccattgtcaaagatcttggttgtgggccatattttttgggcacctatgacaagcgctttccaggctttgtttctccacacaagctcgcctgcgcc atagtcaatacggccggtcgcgagactgggggcgtacactggatggcctttgcctggaacccgcactcaaaaacatgctacctctttgagccc tttggcttttctgaccagcgactcaagcaggtttaccagtttgagtacgagtcactcctgcgccgtagcgccattgcttcttcccccgaccgctgta taacgctggaaaagtccacccaaagcgtacaggggcccaactcggccgcctgtggactattctgctgcatgtttctccacgcctttgccaactg gccccaaactcccatggatcacaaccccaccatgaaccttattaccggggtacccaactccatgctcaacagtccccaggtacagcccaccct gcgtcgcaaccaggaacagctctacagcttcctggagcgccactcgccctacttccgcagccacagtgcgcagattaggagcgccacttcttt ttgtcacttgaaaaacatgtaaaaataatgtactagagacactttcaataaaggcaaatgcttttatttgtacactctcgggtgattatttaccccc acccttgccgtctgcgccgtttaaaaatcaaaggggttctgccgcgcatcgctatgcgccactggcagggacacgttgcgatactggtgtttagtgc tccacttaaactcaggcacaaccatccgcggcagctcggtgaagttttcactccacaggctgcgcaccatcaccaacgcgtttagcaggtcgg gcgccgatatcttgaagtcgcagttggggcctccgccctgcgcgcgcgagttgcgatacacagggttgcagcactggaacactatcagcgcc gggtggtgcacgctggccagcacgctcttgtcggagatcagatccgcgtccaggtcctccgcgttgctcagggcgaacggagtcaactttggt agctgccttcccaaaaagggcgcgtgcccaggctttgagttgcactcgcaccgtagtggcatcaaaaggtgaccgtgcccggtctgggcgtta ggatacagcgcctgcataaaagccttgatctgcttaaaagccacctgagcctttgcgccttcagagaagaacatgccgcaagacttgccggaa aactgattggccggacaggccgcgtcgtgcacgcagcaccttgcgtcggtgttggagatctgcaccacatttcggccccaccggttcttcacg atcttggccttgctagactgctccttcagcgcgcgctgcccgttttcgctcgtcacatccatttcaatcacgtgctccttatttatcataatgcttcc gtgtagacacttaagctcgccttcgatctcagcgcagcggtgcagccacaacgcgcagcccgtgggctcgtgatgcttgtaggtcacctctgcaa acgactgcaggtacgcctgcaggaatcgccccatcatcgtcacaaaggtcttgttgctggtgaaggtcagctgcaacccgcggtgctcctcgtt cagccaggtcttgcatacggccgccagagcttccacttggtcaggcagtagtttgaagttcgcctttagatcgttatccacgtggtacttgtccatc agcgcgcgcgcagcctccatgcccttctcccacgcagacacgatcggcacactcagcgggttcatcaccgtaatttcactttccgcttcgctgg gctcttcctcttcctcttgcgtccgcataccacgcgccactgggtcgtcttcattcagccgccgcactgtgcgcttacctcctttgccatgcttgatt agcaccggtgggttgctgaaacccaccatttgtagcgccacatcttctctttcttcctcgctgtccacgattacctctggtgatggcgggcgctcg ggcttgggagaagggcgcttctttttcttcttgggcgcaatggccaaatccgccgccgaggtcgatggccgcgggctgggtgtgcgcggcac cagcgcgtcttgtgatgagtcttcctcgtcctcggactcgatacgccgcctcatccgcttttttgggggcgcccggggaggcggcggcgacgg ggacggggacgacacgtcctccatggttgggggacgtcgcgccgcaccgcgtccgcgctcgggggtggtttcgcgctgctcctcttcccga ctggccatttccttctcctataggcagaaaaagatcatggagtcagtcgagaagaaggacagcctaaccgccccctctgagttcgccaccacc gcctccaccgatgccgccaacgcgcctaccaccttccccgtcgaggcacccccgcttgaggaggaggaagtgattatcgagcaggaccca ggttttgtaagcgaagacgacgaggaccgctcagtaccaacagaggataaaaagcaagaccaggacaacgcagaggcaaacgaggaaca agtcgggcggggggacgaaaggcatggcgactacctagatgtgggagacgacgtgctgttgaagcatctgcagcgccagtgcgccattatc tgcgacgcgttgcaagagcgcagcgatgtgcccctcgccatagcggatgtcagccttgcctacgaacgccacctattctcaccgcgcgtacc ccccaaacgccaagaaaacggcacatgcgagcccaacccgcgcctcaacttctaccccgtatttgccgtgccagaggtgcttgccacctatc acatctttttccaaaactgcaagatacccctatcctgccgtgccaaccgcagccgagcggacaagcagctggccttgcggcagggcgctgtca tacctgatatcgcctcgctcaacgaagtgccaaaaatctttgagggtcttggacgcgacgagaagcgcgcggcaaacgctctgcaacaggaa aacagcgaaaatgaaagtcactctggagtgttggtggaactcgagggtgacaacgcgcgcctagccgtactaaaacgcagcatcgaggtca cccactttgcctacccggcacttaacctaccccccaaggtcatgagcacagtcatgagtgagctgatcgtgcgccgtgcgcagcccctggaga gggatgcaaatttgcaagaacaaacagaggagggcctacccgcagttggcgacgagcagctagcgcgctggcttcaaacgcgcgagcctg ccgacttggaggagcgacgcaaactaatgatggccgcagtgctcgttaccgtggagcttgagtgcatgcagcggttctttgctgacccggaga tgcagcgcaagctagaggaaacattgcactacacctttcgacagggctacgtacgccaggcctgcaagatctccaacgtggagctctgcaac ctggtctcctaccttggaattttgcacgaaaaccgccttgggcaaaacgtgcttcattccacgctcaagggcgaggcgcgccgcgactacgtcc gcgactgcgtttacttatttctatgctacacctggcagacggccatgggcgtttggcagcagtgcttggaggagtgcaacctcaaggagctgca gaaactgctaaagcaaaacttgaaggacctatggacggccttcaacgagcgctccgtggccgcgcacctggcggacatcattttccccgaac gcctgcttaaaaccctgcaacagggtctgccagacttcaccagtcaaagcatgttgcagaactttaggaactttatcctagagcgctcaggaatc ttgcccgccacctgctgtgcacttcctagcgactttgtgcccattaagtaccgcgaatgccctccgccgctttggggccactgctaccttctgcag ctagccaactaccttgcctaccactctgacataatggaagacgtgagcggtgacggtctactggagtgtcactgtcgctgcaacctatgcaccc cgcaccgctccctggtttgcaattcgcagctgcttaacgaaagtcaaattatcggtacctttgagctgcagggtccctcgcctgacgaaaagtcc gcggctccggggttgaaactcactccggggctgtggacgtcggcttaccttcgcaaatttgtacctgaggactaccacgcccacgagattagg ttctacgaagaccaatcccgcccgccaaatgcggagcttaccgcctgcgtcattacccagggccacattcttggccaattgcaagccatcaaca aagcccgccaagagtttctgctacgaaagggacggggggtttacttggacccccagtccggcgaggagctcaacccaatccccccgccgcc gcagccctatcagcagcagccgcgggcccttgcttcccaggatggcacccaaaaagaagctgcagctgccgccgccacccacggacgag gaggaatactgggacagtcaggcagaggaggttttggacgaggaggaggaggacatgatggaagactgggagagcctagacgaggaag cttccgaggtcgaagaggtgtcagacgaaacaccgtcaccctcggtcgcattcccctcgccggcgccccagaaatcggcaaccggttccag catggctacaacctccgctcctcaggcgccgccggcactgcccgttcgccgacccaaccgtagatgggacaccactggaaccagggccgg taagtccaagcagccgccgccgttagcccaagagcaacaacagcgccaaggctaccgctcatggcgcgggcacaagaacgccatagttgc ttgcttgcaagactgtgggggcaacatctccttcgcccgccgctttcttctctaccatcacggcgtggccttcccccgtaacatcctgcattactac cgtcatctctacagcccatactgcaccggcggcagcggcagcggcagcaacagcagcggccacacagaagcaaaggcgaccggatagc aagactctgacaaagcccaagaaatccacagcggcggcagcagcaggaggaggagcgctgcgtctggcgcccaacgaacccgtatcgac ccgcgagcttagaaacaggatttttcccactctgtatgctatatttcaacagagcaggggccaagaacaagagctgaaaataaaaaacaggtct ctgcgatccctcacccgcagctgcctgtatcacaaaagcgaagatcagcttcggcgcacgctggaagacgcggaggctctcttcagtaaatac tgcgcgctgactcttaaggactagtttcgcgccctttctcaaatttaagcgcgaaaactacgtcatctccagcggccacacccggcgccagcac ctgtcgtcagcgccattatgagcaaggaaattcccacgccctacatgtggagttaccagccacaaatgggacttgcggctggagctgcccaag actactcaacccgaataaactacatgagcgcgggaccccacatgatatcccgggtcaacggaatccgcgcccaccgaaaccgaattctcttg gaacaggcggctattaccaccacacctcgtaataaccttaatccccgtagttggcccgctgccctggtgtaccaggaaagtcccgctcccacc actgtggtacttcccagagacgcccaggccgaagttcagatgactaactcaggggcgcagcttgcgggcggctttcgtcacagggtgcggtc gcccgggcagggtataactcacctgacaatcagagggcgaggtattcagctcaacgacgagtcggtgagctcctcgcttggtctccgtccgg acgggacatttcagatcggcggcgccggccgtccttcattcacgcctcgtcaggcaatcctaactctgcagacctcgtcctctgagccgcgctc tggaggcattggaactctgcaatttattgaggagtttgtgccatcggtctactttaaccccttctcgggacctcccggccactatccggatcaattta ttcctaactttgacgcggtaaaggactcggcggacggctacgactgaatgttaagtggagaggcagagcaactgcgcctgaaacacctggtc cactgtcgccgccacaagtgctttgcccgcgactccggtgagttttgctactttgaattgcccgaggatcatatcgagggcccggcgcacggc gtccggcttaccgcccagggagagcttgcccgtagcctgattcgggagtttacccagcgccccctgctagttgagcgggacaggggaccctg tgttctcactgtgatttgcaactgtcctaaccttggattacatcaagatcctctagttataactagagtacccggggatcttattccctttaactaataa aaaaaaataataaagcatcacttacttaaaatcagttagcaaatttctgtccagtttattcagcagcacctccttgccctcctcccagctctggtattg cagcttcctcctggctgcaaactttctccacaatctaaatggaatgtcagtttcctcctgttcctgtccatccgcacccactatcttcatgttgttgcag atgaagcgcgcaagaccgtctgaagataccttcaaccccgtgtatccatatgacacggaaaccggtcctccaactgtgccttttcttactcctccc tttgtatcccccaatgggtttcaagagagtccccctggggtactctctttgcgcctatccgaacctctagttacctccaatggcatgcttgcgctcaa aatgggcaacggcctctctctggacgaggccggcaaccttacctcccaaaatgtaaccactgtgagcccacctctcaaaaaaaccaagtcaaa cataaacctggaaatatctgcacccctcacagttacctcagaagccctaactgtggctgccgccgcacctctaatggtcgcgggcaacacactc accatgcaatcacaggccccgctaaccgtgcacgactccaaacttagcattgccacccaaggacccctcacagtgtcagaaggaaagctagc cctgcaaacatcaggccccctcaccaccaccgatagcagtacccttactatcactgcctcaccccctctaactactgccactggtagcttgggc attgacttgaaagagcccatttatacacaaaatggaaaactaggactaaagtacggggctcctttgcatgtaacagacgacctaaacactttgac cgtagcaactggtccaggtgtgactattaataatacttccttgcaaactaaagttactggagccttgggttttgattcacaaggcaatatgcaactta atgtagcaggaggactaaggattgattctcaaaacagacgccttatacttgatgttagttatccgtttgatgctcaaaaccaactaaatctaagact aggacagggccctctttttataaactcagcccacaacttggatattaactacaacaaaggcctttacttgtttacagcttcaaacaattccaaaaag cttgaggttaacctaagcactgccaaggggttgatgtttgacgctacagccatagccattaatgcaggagatgggcttgaatttggttcacctaat gcaccaaacacaaatcccctcaaaacaaaaattggccatggcctagaatttgattcaaacaaggctatggttcctaaactaggaactggccttag ttttgacagcacaggtgccattacagtaggaaacaaaaataatgataagctaactttgtggaccacaccagctccatctcctaactgtagactaaa tgcagagaaagatgctaaactcactttggtcttaacaaaatgtggcagtcaaatacttgctacagtttcagttttggctgttaaaggcagtttggctc caatatctggaacagttcaaagtgctcatcttattataagatttgacgaaaatggagtgctactaaacaattccttcctggacccagaatattggaac tttagaaatggagatcttactgaaggcacagcctatacaaacgctgttggatttatgcctaacctatcagcttatccaaaatctcacggtaaaactg ccaaaagtaacattgtcagtcaagtttacttaaacggagacaaaactaaacctgtaacactaaccattacactaaacggtacacaggaaacagg agacacaactccaagtgcatactctatgtcattttcatgggactggtctggccacaactacattaatgaaatatttgccacatcctcttacactttttca tacattgcccaagaataaagaatcgtttgtgttatgtttcaacgtgtttatttttcaattgcagaaaatttcaagtcatttttcattcagtagtatagc cccaccaccacatagcttatacagatcaccgtaccttaatcaaactcacagaaccctagtattcaacctgccacctccctcccaacacacagagtaca cagtcctttctccccggctggccttaaaaagcatcatatcatgggtaacagacatattcttaggtgttatattccacacggtttcctgtcgagccaaa cgctcatcagtgatattaataaactccccgggcagctcacttaagttcatgtcgctgtccagctgctgagccacaggctgctgtccaacttgcggt tgcttaacgggcggcgaaggagaagtccacgcctacatgggggtagagtcataatcgtgcatcaggatagggcggtggtgctgcagcagcg cgcgaataaactgctgccgccgccgctccgtcctgcaggaatacaacatggcagtggtctcctcagcgatgattcgcaccgcccgcagcata aggcgccttgtcctccgggcacagcagcgcaccctgatctcacttaaatcagcacagtaactgcagcacagcaccacaatattgttcaaaatcc cacagtgcaaggcgctgtatccaaagctcatggcggggaccacagaacccacgtggccatcataccacaagcgcaggtagattaagtggcg acccctcataaacacgctggacataaacattacctcttttggcatgttgtaattcaccacctcccggtaccatataaacctctgattaaacatggcg ccatccaccaccatcctaaaccagctggccaaaacctgcccgccggctatacactgcagggaaccgggactggaacaatgacagtggaga gcccaggactcgtaaccatggatcatcatgctcgtcatgatatcaatgttggcacaacacaggcacacgtgcatacacttcctcaggattacaag ctcctcccgcgttagaaccatatcccagggaacaacccattcctgaatcagcgtaaatcccacactgcagggaagacctcgcacgtaactcac gttgtgcattgtcaaagtgttacattcgggcagcagcggatgatcctccagtatggtagcgcgggtttctgtctcaaaaggaggtagacgatccc tactgtacggagtgcgccgagacaaccgagatcgtgttggtcgtagtgtcatgccaaatggaacgccggacgtagtcatatttcctgaagcaaa accaggtgcgggcgtgacaaacagatctgcgtctccggtctcgccgcttagatcgctctgtgtagtagttgtagtatatccactctctcaaagcat ccaggcgccccctggcttcgggttctatgtaaactccttcatgcgccgctgccctgataacatccaccaccgcagaataagccacacccagcc aacctacacattcgttctgcgagtcacacacgggaggagcgggaagagctggaagaaccatgtttttttttttattccaaaagattatccaaaacc tcaaaatgaagatctattaagtgaacgcgctcccctccggtggcgtggtcaaactctacagccaaagaacagataatggcatttgtaagatgttg cacaatggcttccaaaaggcaaacggccctcacgtccaagtggacgtaaaggctaaacccttcagggtgaatctcctctataaacattccagca ccttcaaccatgcccaaataattctcatctcgccaccttctcaatatatctctaagcaaatcccgaatattaagtccggccattgtaaaaatctgctcc agagcgccctccaccttcagcctcaagcagcgaatcatgattgcaaaaattcaggttcctcacagacctgtataagattcaaaagcggaacatt aacaaaaataccgcgatcccgtaggtcccttcgcagggccagctgaacataatcgtgcaggtctgcacggaccagcgcggccacttccccg ccaggaaccttgacaaaagaacccacactgattatgacacgcatactcggagctatgctaaccagcgtagccccgatgtaagctttgttgcatg ggcggcgatataaaatgcaaggtgctgctcaaaaaatcaggcaaagcctcgcgcaaaaaagaaagcacatcgtagtcatgctcatgcagata aaggcaggtaagctccggaaccaccacagaaaaagacaccatttttctctcaaacatgtctgcgggtttctgcataaacacaaaataaaataac aaaaaaacatttaaacattagaagcctgtcttacaacaggaaaaacaacccttataagcataagacggactacggccatgccggcgtgaccgt aaaaaaactggtcaccgtgattaaaaagcaccaccgacagctcctcggtcatgtccggagtcataatgtaagactcggtaaacacatcaggttg attcatcggtcagtgctaaaaagcgaccgaaatagcccgggggaatacatacccgcaggcgtagagacaacattacagcccccataggagg tataacaaaattaataggagagaaaaacacataaacacctgaaaaaccctcctgcctaggcaaaatagcaccctcccgctccagaacaacata cagcgcttcacagcggcagcctaacagtcagccttaccagtaaaaaagaaaacctattaaaaaaacaccactcgacacggcaccagctcaat cagtcacagtgtaaaaaagggccaagtgcagagcgagtatatataggactaaaaaatgacgtaacggttaaagtccacaaaaaacacccaga aaaccgcacgcgaacctacgcccagaaacgaaagccaaaaaacccacaacttcctcaaatcgtcacttccgttttcccacgttacgtaacttcc cattttaagaaaactacaattcccaacacatacaagttactccgccctaaaacctacgtcacccgccccgttcccacgccccgcgccacgtcac aaactccaccccctcattatcatattggcttcaatccaaaataaggtatattattgatgatnnn

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All references, including publications, patent applications, and patents, cited herein are hereby incorporated by reference to the same extent as if each reference were individually and specifically indicated to be incorporated by reference and were set forth in its entirety herein.

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1. A gene transfer vector comprising (i) all or part of a viral genome and (ii) a suicide gene flanked by a first cloning nucleic acid sequence and a second cloning nucleic acid sequence, wherein the first and second cloning nucleic acid sequences are different.
 2. The gene transfer vector of claim 1, wherein the viral genome is an adenovirus genome.
 3. The gene transfer vector of claim 2, wherein the adenovirus genome comprises a deletion of the E1 region.
 4. The gene transfer vector of claim 2, wherein the adenovirus is serotype
 5. 5. The gene transfer vector of claim 1, wherein the suicide gene is a bacterial suicide gene.
 6. The gene transfer vector of claim 5, wherein the bacterial suicide gene is a ccdB gene.
 7. The gene transfer vector of claim 1, wherein each of the first and second cloning nucleic acid sequences comprises about 15-25 nucleotides.
 8. The gene transfer vector of claim 7, wherein each of the first and second cloning nucleic acid sequences comprises about 20 nucleotides.
 9. The gene transfer vector of claim 7, wherein the first cloning nucleic acid sequence comprises SEQ ID NO: 1 (AATCGGAAAGCGGACGCGGA) and the second cloning nucleic acid sequence comprises SEQ ID NO: 2 (CGAGTATCCCGTGAGCGCTT).
 10. (canceled)
 11. A composition comprising the gene transfer vector of claim 1 and a pharmaceutically acceptable carrier.
 12. A system for producing an adenoviral vector, which comprises: (a) a destination vector comprising (i) all or part of an adenoviral genome and (ii) a suicide gene flanked by a first cloning nucleic acid sequence and a second cloning nucleic acid sequence, wherein the first and second cloning nucleic acid sequences are different; (b) a transgene flanked by the first cloning nucleic acid sequence and the second cloning nucleic acid sequence; and (c) reagents for Gibson DNA Assembly (GDA).
 13. The system of claim 12, wherein the adenovirus genome comprises a deletion of the E1 region.
 14. The system of claim 12, wherein the adenovirus is serotype
 5. 15. The system of claim 12, wherein the suicide gene is a bacterial suicide gene.
 16. The system of claim 15, wherein the bacterial suicide gene is a ccdB gene.
 17. The system of claim 12, wherein each of the first and second cloning nucleic acid sequences comprises about 15-25 nucleotides.
 18. The system of claim 17, wherein each of the first and second cloning nucleic acid sequences comprises about 20 nucleotides.
 19. The system of claim 17, wherein the first cloning nucleic acid sequence comprises SEQ ID NO: 1 (AATCGGAAAGCGGACGCGGA) and the second cloning nucleic acid sequence comprises SEQ ID NO: 2 (CGAGTATCCCGTGAGCGCTT).
 20. (canceled)
 21. A method of producing an adenoviral vector comprising contacting a cell with the system of claim
 12. 